chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48596203685962037CG16GENIChomozygous145474933
48596302685963027A20GENIChomozygous141114890
48596306585963066CA23GENIChomozygous137110650
48596496685964967AG24GENIChomozygous137110653
48596581285965813GT23GENIChomozygous145474934
48596617785966178CT23GENIChomozygous145474935
48596684385966844AT9GENIChomozygous145474936
48596838885968389CG21GENIChomozygous145474937
48596845385968454AG28GENIChomozygous145474938
48596903885969039GA19GENIChomozygous137110655
48596976285969763GA19GENIChomozygous137110656
48597002585970026CG31GENIChomozygous137110657
48597076285970763CT22GENIChomozygous137110660
48597155485971555AC13GENIChomozygous145474939
48597561485975615TC21GENIChomozygous137110665
48597041885970419TC27GENIChomozygous143101930
48597925285979253C6GENIChomozygous136897122
48598228985982290TG14GENIChomozygous145474940
48598362885983629GT12GENIChomozygous145474941
48598466285984663G16GENIChomozygous145441814
48598466585984666TA15GENIChomozygous145474942
48598577485985775CT24GENIChomozygous145474943
48598826585988266AG15GENIChomozygous137110679
48599075285990753CT24GENIChomozygous145474944
48599099985991000GA18GENIChomozygous137110684
48599830485998305GA21GENIChomozygous145474946
48599390385993904TC23GENIChomozygous137110688
48599406685994067GA16GENIChomozygous137110689
48599602385996024GC30GENIChomozygous145474945
48599994585999946CT28GENIChomozygous137110695
48600108086001081GA26GENIChomozygous145474947
48600231286002313CT25GENIChomozygous145474948