Based on the comments from Wendy Krieger below, I accept this observation from მამუკა ჯიბლაძე as an acceptable answer to the question
      
"product of all coordinates is 1 for E, -1 for O and 0 for A"
     
Comments from Wendy Krieger 11/06/2018:

    There is a geometric description here, which has to deal with 
    reflections.  A reflection in a mirror will produce a reversed image, 
    that is, convert 1 to -1.
        
    If you place two mirrors at right-angles, the image in the corner is a 
    double reflection, or -1 * -1 = +1.  So if you looked at yourself in 
    this arrangement, when you lift your right hand, the image lift its 
    right hand too.  In a single reflection, a right hand is reflected to 
    the image's left hand.
       
    The most likely source for this is the rectangular mirrors (the ones 
    like x=0, and y=0, and z=0), are flipping the image back and forward. 
    What it probably means in terms of your experiment is that A-X and A+X 
    somehow add to the same measure, but the difference from A is being 
    inverted.
        
    The whole of E8 is a eutactic star.  The two 24-cells are eutactic 
    stars, severally and jointly, and the thing you are looking at is one of 
    the 16chora inscribed in the 24-cells.
    
    The 24ch is the group of order 192, can be divided into three 4r's 
    (16ch) or lines at right angles.  These three can be labeled say N, E, 
    O.  The vertices of the form (1,1,1,1) etc, can be formed by an 'even' 
    sum of four N axies, or an odd sum of four O axies. even and odd here 
    means that the axies are labeled as +1 to -1, and an e/o number of 
    negatives are used.
         
    Likewise, (2,0,0,0) can be formed by an 'even' number of E or an 'odd' 
    number of O vectors.
       
    The signs then correspond to reflections in the N star, which inverts 
    exactly one axis (eg w,x,y,z -> -w,x,y,z) and to get to other points, 
    you have to reflect in the x, y, and/or z mirror too.
       
    The progression from O to N to E is a linear operation in odd 
    dimensions, but involves some sort of turn in even ones.  This is why 
    they can be treated symmetrically in 4 and 8 dimensions.

Added 20 Dec 2018:

For those familiar with at least the rudiments of biomolecular translation (the process by which messages transcribed from genes are translated into proteins), the following conceptual cheat-sheet may help explain why an affirmative answer to the "generalized Kronecker delta" question was so important to my research team.  In order to be able to deliver on the claims made in this cheat-sheet, we needed to be able to show that given Wendy's construction, we can define a "high" (+1), "low" (-1), and a midpoint between them (0).  And the affirmative answer provided to the question by  @მამუკაჯიბლაძე tells us that this is possible. 

    Conceptual Cheat-Sheet
    
    Our analysis deals solely with sets of dicodons and the sets of dipeptides
    they encode, NOT with individual codons and encoded amino acids, nor with 
    individual dicodons and encoded dipeptides.   
    
    Our analysis deals solely with the energetic properties of sets of dicodons,
    the affinity properties of sets of dipeptides (hydrophobicity), and the 
    synthetase affiliation properties of sets of dipeptides (Class I or Class 
    II).  No other properties of dicodons or dipeptides are relevant to the
    analysis.
    
    Our analysis identifies certain energetic symmetries in the energetic 
    patterns exhibited by our sets  of dicodons.
    
    Our analysis identifies certain affinity symmetries in the affinity patterns
    exhibited by our sets of dipeptides.
    
    Our analysis identifies certain affiliation symmetries in the affiliation 
    patterns exhibited by our sets of dipeptides.
    
    Our analysis identifies certain consistent symmetry relations between 
    energetic symmetries and affinity symmetries, and also between energetic 
    symmetries and affiliation symmetries.
    
    These symmetry relations hold for: i) both amino acids of dipeptides (AA1 
    and AA2 in a dipeptide AA1AA2); or ii) AA1 only; or iii) AA2 only; or iv) 
    neither.  And we interpret (i-iv) as suggesting that sets of dipeptides 
    assumed functionality in protein structure according to this rough 3-way 
    chronology:
    
    	Early onset of functionality: 	sets of dipeptides exhibiting symmetry
                                        relations to their dicodon sets for both 
                                        AA1And AA2
    	Late onset of functionality:	sets of dipeptides exhibiting symmetry
                                        relations to their dicodon sets for 
                                        neither AA1 nor AA2
    	Onset midway:			        sets of dipeptides exhibiting symmetry 
                                        relations to their dicodon set for AA1
                                        or AA2 but not botj
    
    Our rationale for this chronology is that early onset dipeptide sets assumed 
    functionality when mRNA energetics were still important in early translation
    systems, whereas late onset dipeptides assumed functionality in relatively 
    mature translation systems in which mRNA energetics were relatively less 
    important (primarily due to the advent of the water-tight ribosome.)
    
    This hypothetical chronology is fully falsifiable by determining if it makes
    correct predictions with respect to “early-late” pairs of SCOP protein 
    families within SCOP superfamilies (where protein family age is taken as the
    ranking assigned by GCA and his team.)

Added 12/30/2018:

Since the 72 vertices of the polytope 1_22 occur as 72 of the 240 vertices of the polytope 4_21 (corresponding to the fact that the roots of E8 contain a copy of the roots of E6), Dr. Richard Klitzing kindly investigated whether there might be an empirically relevant construction inside 1_22 which might be intrinsically related to Wendy Krieger's empirically relevant tetrahedral construction within 4_21.  Richard has determined that in 1_22, one can find 40 pairs of opposed pentachora (aka 5-cells, aka hypertetrahedrons in 4-space) and these 40 pairs seem to be empirically relevant to our biomolecular results.  However, Richard and Wendy have not yet determined whether Richard's pentachora are related to Wendy's tetrahedra in any meaningful way.  Also, note that this question is a new particular version of the more general question asked in this post last year:  https://mathoverflow.net/questions/288114/e-6-e-8-and-coxeters-anti-prismatic-projections-of-the-n-dimensional-cr

Here are further details on the pentachora from Richard, in reponse to my question to him as to whether his 40 pairs of pentachora can be divided into three subsets of 10, 20, and 10.

    Those 2 x 40 pentachora within that E_6 figure 1_22 (= mo) had been obtained 
    from its D_5 subsymmetry, when being seen as hin (= 1_21, hemipenteract) 
    atop rat (rectified 5D crosspolytope) atop alternate hin (i.e. the “other” 
    hemipenteract) as xoo3ooo3oox *b3oxo3ooo&#xt. In fact, each hemipenteract 
    layer shows up 40 tetrahedra which are solely connected to hexadecachora 
    (within that very layer). (In fact, those are the following tetrahedra: 
    x3o3o *b3.3.) Those tetrahedra furthermore connect to the medial layer 
    (featuring exactly 40 vertices) via tips, thus becoming pyramids with 
    tetrahedral bases, aka the mentioned pentachora.
    
    Now you ask whether those 40 pentachora (on either side) would be divisable
    into a sum of 10+20+10. Thus your question readily is transfering down one
    dimension, yielding the quest to divide those 40 tetrahedra within either hin.
     
    And indeed, when considering hin in turn as an axial stack (aka lace tower)
    of a point atop a rectified penteract atop a (relatively inverted) penteract,
    i.e. in axial A_4 symmetry, as ooo3oxo3ooo3oox&#xt, then those 40 tetrahedra
    show up as
    
      10x  oo.3ox.3...3...&#xt
      20x  ...3.xo3.oo3...&#xt
      10x  ...3...3.oo3.ox&#xt
    
    which is nothing but a positive answer to your quest.
     
    Thus in total you break the E_6 symmetry down into a lace city (i.e. a 2D 
    position space) with a 4D perpendicular object space. That perp space then 
    still features A_4 symmetry. (Btw., the corresponding position space 
    geometry is readily visible displayed as the 2nd provided lace city of 
    https://bendwavy.org/klitzing/incmats/mo.htm.)

And here is my response to Richard:

    Thank you very much, Richard!
    
    I am very glad that there is an affirmative answer to the question, 
    because it arose from a consideration of this empirically derived table:
    
                  Min
    Asym    2       1       0	
    
    yr>ry   1       5       3        9
    yr=ry   8       9       2       19
    yr<ry   1       6       5       12
           10      20      10       40
    
    I won't bother at the moment to tell you what the counts in this 
    matrix are - it's too complicated for a short email.)
    
    But I do want to draw your attention to the fact that the 3x3 matrix here
    is our empirical counterpart to Wendy's 3x3 matrix from which her three 
    sets of 16 tetrahedra can be selected in 6 different ways.
    
    And in my own personal opinion, the fact that we get these 10-20-10 
    column sums strongly suggests that your pentachora in 1_22 (E6) 
    can in fact be systematically related to Wendy's tetrahedra in 4_21 (E8), 
    assuming of couse that we choose to locate the1_22 inside a 4_21  
    (i.e. to locate a copy of the roots of E6 inside the roots of E8.)