chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107507760875077609T-4GENICheterozygous51912466
107507914575079146CCTTT10GENICheterozygous52386176
107507914675079147T-10GENICheterozygous51912468
107510836175108363AA--13GENIChomozygous52321312
107510836375108364AATTTT13GENIChomozygous52321314
107510886275108863G-6GENICheterozygous51497936
107511175775111758C-7GENICpossibly homozygous51497939
107511179475111795A-4GENICheterozygous51497940
107511750575117506CA10GENICheterozygous51497948
107512995275129958ATTTGG------21GENIChomozygous51497968
107513070175130703CA--20GENICheterozygous52386192
107513302675133027TTC10GENICheterozygous52386194
107511207375112074T-11GENICheterozygous51697321
107511844075118441TG15GENIChomozygous51697325
107513855975138561AT--10GENICpossibly homozygous51697329
107514046275140463AAT6GENICheterozygous51497982