chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161893486161893486ATAC11GENICpossibly homozygous136926568
4161893712161893712CATACACACA7GENIChomozygous136926569
4161893841161893842C15GENIChomozygous136926570
4161894455161894456CT19GENIChomozygous137254661
4161896652161896653AG17GENIChomozygous137254662
4161898382161898383A14GENIChomozygous136926571
4161899943161899944CT10GENIChomozygous137254663
4161901492161901493CT15GENIChomozygous137254664
4161903309161903311AA13GENIChomozygous136926572
4161903792161903793AG7GENIChomozygous137254665
4161903859161903860A2GENIChomozygous136926573
4161903860161903861AG2GENIChomozygous137254666
4161903863161903864GT3GENIChomozygous137254667
4161903912161903913CT8GENIChomozygous137254668
4161903923161903924GA8GENIChomozygous137254669
4161903935161903936GA9GENIChomozygous137254670