chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161892066161892067AC17GENICheterozygous154222710
4161892066161892067AT17GENIChomozygous154222711
4161893486161893486ATAC13GENICpossibly homozygous136926568
4161893712161893712CATACACACA17GENICheterozygous136926569
4161893841161893842C21GENIChomozygous136926570
4161894455161894456CT25GENIChomozygous137254661
4161896652161896653AG20GENIChomozygous137254662
4161898382161898383A28GENIChomozygous136926571
4161899943161899944CT20GENIChomozygous137254663
4161901492161901493CT21GENIChomozygous137254664
4161903309161903311AA19GENIChomozygous136926572
4161903792161903793AG16GENIChomozygous137254665
4161903859161903860A13GENIChomozygous136926573
4161903860161903861AG13GENIChomozygous137254666
4161903863161903864GT14GENIChomozygous137254667
4161903912161903913CT19GENIChomozygous137254668
4161903923161903924GA19GENIChomozygous137254669
4161903935161903936GA21GENIChomozygous137254670