chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116928822116928823AC40GENIChomozygous115845859
7116930571116930572TC65GENIChomozygous115845861
7116930950116930951TC55GENIChomozygous115845863
7116931640116931641TC58GENIChomozygous115845865
7116932522116932523GA59GENIChomozygous115845867
7116932532116932533GA58GENIChomozygous115845869
7116933057116933058AT61GENICpossibly homozygous115845871
7116933972116933973AG53GENIChomozygous115845873
7116934411116934412GA60GENIChomozygous115845875
7116935780116935781GT54GENIChomozygous115845877
7116937285116937286GT57GENIChomozygous115845879
7116939739116939740TG59GENIChomozygous115845881
7116941317116941318TC59GENIChomozygous115845883
7116941522116941523AG52GENIChomozygous115845885
7116941528116941529TA50GENIChomozygous115845887
7116941529116941530CA50GENIChomozygous115845889
7116941720116941721CA72GENICpossibly homozygous115845891
7116941721116941722TG72GENICpossibly homozygous115845893
7116930772116930773T60GENIChomozygous128510394
7116939505116939505CTG54GENIChomozygous128510395
7116941685116941686A61GENICpossibly homozygous128510396