chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81435961014359611AC60GENIChomozygous117957895
81436017414360175AG45GENIChomozygous117957896
81436062114360622CT40GENIChomozygous117957897
81436063614360637CT39GENIChomozygous117957898
81436066914360670TC40GENIChomozygous117957899
81436103814361039CT54GENIChomozygous117957900
81436146514361466CT51GENIChomozygous117957901
81436157914361580CT57GENIChomozygous117957902
81436206414362065GA56GENIChomozygous117957903
81436215614362157GA51GENIChomozygous117957904
81436369214363693TC49GENIChomozygous117957905
81436509814365099CG57GENIChomozygous117957906
81436546714365468CT58GENIChomozygous117957907
81436604014366041AT53GENIChomozygous117957908
81436619014366191GC61GENIChomozygous117957909
81436701614367017CT51GENIChomozygous117957910
81436765914367660CT47GENIChomozygous117957911
81436776314367764TC62GENIChomozygous117957912
81436821114368212GA53GENIChomozygous117957913
81436851414368515AG44GENIChomozygous117957914
81436882214368823TC48GENIChomozygous117957915
81436891914368920TC38GENIChomozygous117957916
81436932114369322GA50GENIChomozygous117957917
81437093514370936AT56GENIChomozygous117957918
81437151814371519GA63GENIChomozygous117957919
81437182714371833AGGATG47GENIChomozygous132871877
81436020214360202TGTGTT25GENICheterozygous132871872
81436020414360204TGTT30GENICheterozygous132871873
81436486714364867A43GENICpossibly homozygous132871874
81436494814364953TTCTC61GENIChomozygous132871875
81436932314369324C49GENIChomozygous132871876
81436349514363496GA48GENIChomozygous132875461
81436835614368357CT64GENIChomozygous116434496
81437215114372152A56GENIChomozygous128572452
81437216914372169CAGA51GENIChomozygous128572453
81437233214372333GA49GENIChomozygous116434497
81437257614372577CT59GENIChomozygous117957920
81437305914373060CT48GENIChomozygous117957921
81437344114373442G65GENIChomozygous128572454
81437346814373469GT71GENIChomozygous116434499
81437368014373681GA63GENIChomozygous116434500