chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1125213182125213183CA22GENIChomozygous959940653
1125213926125213927CT30GENIChomozygous959940654
1125214231125214232TC28GENIChomozygous959940655
1125214871125214872AG17GENIChomozygous959940656
1125214953125214954CT18GENIChomozygous959940657
1125215239125215240GA22GENIChomozygous959940658
1125215695125215696GA9GENIChomozygous959940659
1125217485125217486GA47GENIChomozygous959940660
1125218976125218977TC29GENIChomozygous959940661
1125221356125221357CT29GENIChomozygous959940662
1125224111125224112CT28GENIChomozygous959940663
1125224413125224414AG40GENIChomozygous959940664
1125226171125226172TC20GENIChomozygous959940665
1125226820125226821GA27GENIChomozygous959940666
1125226862125226863GA23GENIChomozygous959940667
1125226934125226935GA22GENIChomozygous959940668
1125226967125226968CT25GENIChomozygous959940669
1125227266125227267CA21GENIChomozygous959940670
1125227267125227268CA21GENIChomozygous959940671
1125227268125227269CT21GENIChomozygous959940672
1125227524125227525CA23GENIChomozygous959940673
1125227655125227656GA23GENIChomozygous959940674
1125228013125228014TC27GENIChomozygous959940675
1125228026125228027AC30GENIChomozygous959940676
1125228141125228142GT18GENIChomozygous959940677
1125228215125228216CT17GENIChomozygous959940678
1125228275125228276CG15GENIChomozygous959940679
1125228284125228285TA16GENIChomozygous959940680
1125228363125228364TC21GENIChomozygous959940681
1125228434125228435TC21GENIChomozygous959940682
1125228819125228820CT15GENIChomozygous959940683
1125228884125228885AG15GENIChomozygous959940684
1125228896125228897TC17GENIChomozygous959940685