chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187577222275772223CT65GENIChomozygous147168979
187577298475772985AG75GENIChomozygous147168980
187577404575774046TC46GENIChomozygous147168981
187577412375774124TA40GENIChomozygous147168982
187577451175774512AG52GENIChomozygous147168983
187577606675776067GC45GENIChomozygous147168984
187577610975776110TC52GENIChomozygous147168985
187577616275776163GA54GENIChomozygous147168986
187577624575776246CT62GENIChomozygous147168987
187577643675776437AG67GENIChomozygous147168988
187577661275776613CT44GENIChomozygous147168989
187577702975777030GA24GENICpossibly homozygous147168990
187577710475777105GA23GENIChomozygous147168991
187577731175777312CT45GENIChomozygous147168992
187577743375777434GA39GENIChomozygous147168993
187577826975778270GA52GENIChomozygous147168994
187577928875779289TG38GENIChomozygous147168995
187577931675779316GT34GENIChomozygous147158179
187577832675778327T50GENIChomozygous141146592
187577843275778434AT19GENIChomozygous147158178
187578133475781335GA45GENIChomozygous147168996
187578383875783839CG62GENIChomozygous147168997
187578449475784495AG52GENIChomozygous147168998
187578522875785229TC40GENIChomozygous147168999
187578721275787213CT57GENIChomozygous147169000
187577843575778436CG21GENICpossibly homozygous155056203
187577843575778436C21GENICheterozygous403674225
187578755875787559GC77GENIChomozygous147169001