chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161892066161892067AC46GENICheterozygous154222710
4161892066161892067AT46GENIChomozygous154222711
4161893486161893486ATAC38GENICpossibly homozygous136926568
4161893712161893712CATACACACA22GENICheterozygous136926569
4161893841161893842C29GENIChomozygous136926570
4161898382161898383A38GENIChomozygous136926571
4161903309161903311AA39GENIChomozygous136926572
4161899943161899944CT44GENIChomozygous137254663
4161903792161903793AG47GENIChomozygous137254665
4161894455161894456CT55GENIChomozygous137254661
4161896652161896653AG52GENIChomozygous137254662
4161901492161901493CT41GENIChomozygous137254664
4161903859161903860A44GENIChomozygous136926573
4161903860161903861AG47GENIChomozygous137254666
4161903863161903864GT47GENIChomozygous137254667
4161903912161903913CT49GENIChomozygous137254668
4161903923161903924GA48GENIChomozygous137254669
4161903935161903936GA50GENIChomozygous137254670