chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91430397914303980CT19GENIChomozygous51762438
91430399614303997C-19GENIChomozygous51762440
91430409114304092AG15GENIChomozygous51762442
91430464914304650GA17GENIChomozygous51762444
91430518314305184TC12GENIChomozygous51762446
91430524114305242T-7GENIChomozygous51762448
91430538014305381CG14GENIChomozygous51762450
91430584614305847G-18GENICpossibly homozygous51762452
91430592414305925AG22GENIChomozygous51762454
91430680214306803CT14GENIChomozygous51762458
91430688614306887AG13GENIChomozygous51762460
91430689314306894TC13GENIChomozygous51762462
91430772014307721GA15GENIChomozygous51762464
91430804214308043GA7GENIChomozygous51762468
91430847614308477CA8GENIChomozygous51762476
91430850114308502TC10GENIChomozygous51762478
91430899314308994CT20GENIChomozygous51762480
91430914214309143GGACGA14GENIChomozygous51762482
91430958814309589TC16GENIChomozygous51762484
91431156614311567AG16GENIChomozygous51762486
91431196714311968TC11GENIChomozygous51762488
91431238114312382CT9GENIChomozygous51762490
91431280714312808TC12GENIChomozygous51762494
91431421214314213G-13GENIChomozygous51762496
91431455114314552AT14GENIChomozygous51762498