chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106406236464062365TC45GENIChomozygous116616812
106406350764063508TC41GENIChomozygous116616814
106406364264063643AG44GENICpossibly homozygous116616816
106406449164064492TG39GENIChomozygous116616818
106406468564064686AG39GENIChomozygous116616820
106406514364065144TC34GENIChomozygous116616822
106406534464065345GA59GENIChomozygous117151148
106406563664065637GA62GENIChomozygous116616826
106406569864065699GT55GENIChomozygous117151150
106406645964066460TC44GENIChomozygous116616828
106406652464066525CG36GENIChomozygous117151151
106406653764066538GA33GENIChomozygous117151152
106406654364066544GA32GENICpossibly homozygous117151153
106406722864067229TC30GENIChomozygous117998350
106406749864067499GA46GENIChomozygous116616832
106406776364067764CT48GENIChomozygous116616834
106406782664067827CA55GENIChomozygous116616836
106406796464067965GT46GENIChomozygous116616838
106406845364068454GA42GENIChomozygous116616840
106406854364068544CT45GENIChomozygous116616842
106406857564068576GA50GENIChomozygous116616844
106406934564069346GA58GENIChomozygous117151154
106406952764069528TC36GENIChomozygous116616848
106406979764069798CA49GENIChomozygous116616850
106407082064070821AG40GENIChomozygous116616852
106407099664070997GT45GENICheterozygous117079984
106407125564071256TG36GENIChomozygous117151155
106407158864071589AG50GENIChomozygous117062340
106407211964072120CT49GENICpossibly homozygous117062344
106407275764072758CT31GENIChomozygous116616856