chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65059774950597750GA26GENIChomozygous118609194
65059778350597784AG35GENIChomozygous114797606
65059801450598015GA31GENIChomozygous118609195
65059843750598438GA19GENIChomozygous114797608
65059878050598781AG29GENIChomozygous114797611
65059896650598967AT29GENIChomozygous114797612
65059897450598975TA28GENIChomozygous114797613
65059911450599115CA15GENIChomozygous114797614
65060266050602661TC21GENIChomozygous114797630
65060308550603086AC26GENIChomozygous114797632
65060332950603330CT28GENIChomozygous118609196
65060544150605442TA35GENIChomozygous114797634
65060632850606329AT23GENIChomozygous118609197
65060665350606654AG32GENIChomozygous114797636
65060669450606695AT33GENIChomozygous114797637
65060676450606765CT36GENIChomozygous114797638
65060681350606814CA31GENICpossibly homozygous118585537
65060681450606815TC32GENICpossibly homozygous118585538
65060731250607313CT27GENIChomozygous114797639
65060801450608015CT27GENIChomozygous114797640
65060902150609022TC19GENIChomozygous114797642
65060991150609912GA30GENIChomozygous114797643
65060997550609976CA28GENIChomozygous114797644
65061011150610112CT24GENIChomozygous114797645
65061030650610307CG36GENIChomozygous114797646
65061032550610326CT31GENIChomozygous114797647
65061151050611511CA33GENIChomozygous114797648
65061218150612182TC22GENIChomozygous114797649
65061236350612364CT21GENICpossibly homozygous118609198
65061279650612797AC25GENIChomozygous114797650
65061356950613570GA15GENIChomozygous114797652
65061367350613674CT22GENIChomozygous114797653
65061518250615183CT21GENIChomozygous114797655
65061579450615795AG25GENIChomozygous114797656
65061593650615937CA27GENIChomozygous114797657
65061632250616323CT29GENICpossibly homozygous118609199
65061649050616491GC25GENIChomozygous114797658
65061655050616551CT29GENIChomozygous114797659
65061754050617541CA31GENIChomozygous114797661
65061793550617936CA26GENIChomozygous114797662
65061810150618102AG14GENIChomozygous118553398
65061846250618463GC12GENIChomozygous114797663