chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2094183379418338TTGAGTGTTGA18GENIChomozygous45679705
2094183839418384GA25GENICpossibly homozygous45679706
2094184339418434TG33GENIChomozygous45679708
2094186469418647TA37GENIChomozygous45679710
2094192259419226TA33GENIChomozygous45679712
2094192319419249GATGTAGGCTTACACTCA------------------20GENIChomozygous45679714
2094192489419249A-26GENIChomozygous45679715
2094194179419418GA48GENIChomozygous45679717
2094195099419510AG59GENICpossibly homozygous45679719
2094202849420285GA30GENIChomozygous45679720
2094202939420294CT25GENIChomozygous45679722
2094203139420314CT24GENIChomozygous45679723
2094203239420324TC23GENIChomozygous45679725
2094203509420357TTTTTTT-------17GENIChomozygous45679727
2094203689420369CCT20GENIChomozygous45679728
2094204229420423AG42GENIChomozygous45679730
2094205769420577CA59GENIChomozygous45679732
2094206929420693CG32GENICheterozygous45423423
2094207609420761TA42GENIChomozygous45679733
2094208899420890GGTCAA28GENIChomozygous45679735
2094209499420950GA39GENIChomozygous45679736
2094209909420991AT45GENIChomozygous45679738
2094210149421015AG45GENIChomozygous45679739
2094211609421161CCCT37GENIChomozygous45679741
2094212359421236CT46GENICpossibly homozygous45679743
2094213929421393AG25GENIChomozygous45679744
2094218679421868GA32GENIChomozygous45679746
2094219169421917TA42GENIChomozygous45679747
2094219479421948TG42GENIChomozygous45679749
2094219749421975TA51GENIChomozygous45679751
2094221609422161TC41GENIChomozygous45423424
2094222179422218CT33GENIChomozygous45679753
2094222369422237GA35GENIChomozygous45679754
2094223259422326AG14GENIChomozygous45679756
2094223769422377GT12GENICpossibly homozygous45756572
2094224209422421TC6GENIChomozygous45679757
2094225119422512GGC8GENIChomozygous45679759
2094225839422584CG16GENICpossibly homozygous45423426
2094226679422668GA19GENIChomozygous45756573