chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103577020435770205GT21GENICpossibly homozygous116558420
103577052735770528T13GENIChomozygous128807414
103577053335770533T13GENIChomozygous128807415
103577055135770551A14GENIChomozygous128807416
103577058235770583AG15GENIChomozygous116558422
103577063535770636A3GENIChomozygous128807417
103577066735770668CG3GENIChomozygous128867707
103577077535770777CC27GENIChomozygous128807418
103577143435771435TC14GENIChomozygous116558424
103577277535772776TC18GENIChomozygous116558426
103577445935774459T12GENIChomozygous128807419
103577915035779151CT22GENIChomozygous116558428
103578104635781047CG18GENIChomozygous116558430
103578104735781048TC17GENIChomozygous116558432
103578252735782528AG15GENIChomozygous116558434
103578253335782534A15GENIChomozygous128807420
103578702135787022GC24GENIChomozygous116558436
103578709335787094GC22GENIChomozygous116558438
103578713435787135CT21GENIChomozygous116558440
103578944135789442GA37GENIChomozygous116558450
103578809935788100AG17GENIChomozygous116558442
103578843635788437CT22GENIChomozygous116558444
103578858635788587GC23GENIChomozygous116558446
103578885535788856CT31GENIChomozygous116558448
103579100835791009TA24GENIChomozygous116558452
103579424235794243GA16GENIChomozygous116558454
103579511235795113AT11GENIChomozygous116558456
103579555335795554TG27GENIChomozygous116558458
103579564235795643CT25GENIChomozygous116558460
103579724335797244TC18GENIChomozygous116558462
103579807535798076TC21GENIChomozygous116558464
103579946535799466CT18GENIChomozygous116558466
103579948435799485GC16GENIChomozygous116558468
103580043035800431TC15GENIChomozygous116558470
103580046635800467AC20GENIChomozygous116558472
103579952735799528TG19GENIChomozygous116977062
103579956835799569CG20GENIChomozygous116977064
103579959235799593CG19GENIChomozygous117103274
103579959835799599CG19GENIChomozygous117170719