chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65059778350597784AG27GENIChomozygous114797606
65059843750598438GA21GENIChomozygous114797608
65059854450598545AG12GENIChomozygous114797609
65059862750598628GA19GENIChomozygous114797610
65059878050598781AG32GENIChomozygous114797611
65059896650598967AT24GENIChomozygous114797612
65059897450598975TA23GENIChomozygous114797613
65059911450599115CA31GENIChomozygous114797614
65060266050602661TC19GENIChomozygous114797630
65060272350602724AT20GENIChomozygous114797631
65060308550603086AC19GENIChomozygous114797632
65060357650603577GC21GENIChomozygous114797633
65060544150605442TA21GENIChomozygous114797634
65060546550605466CT23GENIChomozygous114797635
65060665350606654AG41GENIChomozygous114797636
65060669450606695AT41GENIChomozygous114797637
65060676450606765CT37GENIChomozygous114797638
65060731250607313CT22GENIChomozygous114797639
65060801450608015CT13GENIChomozygous114797640
65060854850608549GA21GENIChomozygous114797641
65060902150609022TC20GENIChomozygous114797642
65060991150609912GA30GENIChomozygous114797643
65060997550609976CA26GENIChomozygous114797644
65061011150610112CT24GENIChomozygous114797645
65061030650610307CG20GENIChomozygous114797646
65061032550610326CT17GENIChomozygous114797647
65061151050611511CA22GENIChomozygous114797648
65061218150612182TC18GENIChomozygous114797649
65061279650612797AC27GENIChomozygous114797650
65061356950613570GA21GENIChomozygous114797652
65061367350613674CT24GENIChomozygous114797653
65061472150614722GA32GENIChomozygous114797654
65061518250615183CT24GENIChomozygous114797655
65061579450615795AG29GENIChomozygous114797656
65061593650615937CA26GENIChomozygous114797657
65061649050616491GC18GENIChomozygous114797658
65061655050616551CT15GENIChomozygous114797659
65061700150617002GA15GENIChomozygous114797660
65061754050617541CA20GENIChomozygous114797661
65061793550617936CA37GENIChomozygous114797662
65061861450618615TC20GENIChomozygous114797664