chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064692510646926AG40GENIChomozygous109993981
191064696310646964TC36GENIChomozygous109634593
191064718610647187GA23GENIChomozygous109993984
191064739010647391AG16GENICheterozygous110122790
191064752710647528TC23GENICpossibly homozygous109993986
191064758610647587CT17GENICpossibly homozygous109993989
191064927310649274CT43GENIChomozygous109993991
191065027810650279GA25GENIChomozygous109993993
191065101110651012TA25GENIChomozygous109993995
191065108910651090GA28GENIChomozygous109993998
191065185010651851CG34GENIChomozygous109994000
191065202510652026TC21GENIChomozygous109634670
191065254610652547TC34GENIChomozygous109634678
191065255410652555TA34GENIChomozygous109634680
191065301010653011AG26GENIChomozygous119711062
191065363310653634CT30GENIChomozygous109994002
191065401510654016TG16GENIChomozygous109634686
191065418910654190GC18GENIChomozygous109634688