chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106406236464062365TC24GENIChomozygous116616812
106406350764063508TC35GENIChomozygous116616814
106406364264063643AG33GENIChomozygous116616816
106406449164064492TG32GENIChomozygous116616818
106406468564064686AG47GENICpossibly homozygous116616820
106406514364065144TC20GENIChomozygous116616822
106406534464065345GA32GENIChomozygous117151148
106406563664065637GA19GENIChomozygous116616826
106406569864065699GT19GENICpossibly homozygous117151150
106406645964066460TC45GENIChomozygous116616828
106406652464066525CG39GENIChomozygous117151151
106406653764066538GA38GENIChomozygous117151152
106406654364066544GA38GENIChomozygous117151153
106406722864067229TC30GENICpossibly homozygous117998350
106406749864067499GA31GENIChomozygous116616832
106406776364067764CT25GENIChomozygous116616834
106406782664067827CA35GENIChomozygous116616836
106406796464067965GT28GENIChomozygous116616838
106406845364068454GA40GENIChomozygous116616840
106406854364068544CT30GENIChomozygous116616842
106406857564068576GA29GENIChomozygous116616844
106406934564069346GA34GENIChomozygous117151154
106406952764069528TC30GENIChomozygous116616848
106406979764069798CA44GENIChomozygous116616850
106407082064070821AG46GENIChomozygous116616852
106407099664070997GT46GENICheterozygous117079984
106407125564071256TG30GENIChomozygous117151155
106407158864071589AG17GENIChomozygous117062340
106407211964072120CT50GENIChomozygous117062344
106407275764072758CT26GENIChomozygous116616856