chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122219619222196193AG10GENIChomozygous115280633
122219620322196204CT12GENIChomozygous115280635
122219646422196465AG11GENIChomozygous115280637
122219650722196508GA13GENIChomozygous115280639
122219668622196687CT15GENIChomozygous115280641
122219796222197963AG10GENICpossibly homozygous115280643
122219806622198067GA5GENIChomozygous115280645
122219807322198074TC5GENIChomozygous115280647
122219855022198551CA5GENIChomozygous115280649
122219866722198668GT3GENIChomozygous115280651
122220041622200417AG8GENIChomozygous115280655
122220059622200597GA5GENIChomozygous115280657
122220153622201537AG12GENIChomozygous115280659
122220221322202214AC9GENIChomozygous115280661
122220229622202297GA9GENIChomozygous115280663
122220316022203161GA4GENIChomozygous115280665
122220332122203322TC13GENIChomozygous115280667
122220363522203636GA12GENIChomozygous115280669
122220365922203660CT15GENIChomozygous115280671
122220376122203762GA12GENIChomozygous115280673
122220382622203827AG12GENIChomozygous115280675
122220419122204192CA9GENIChomozygous115280677
122220498022204981TA5GENIChomozygous115280679
122220825322208254CT9GENIChomozygous115280681
122220950622209507TC9GENIChomozygous115280687
122221021722210218AG10GENIChomozygous115280691
122221068322210684AG5GENIChomozygous115366503
122220756422207565AG4GENIChomozygous115366497
122220862922208630GA13GENIChomozygous115366499
122220907622209077CT10GENIChomozygous115366501
122221075122210752CT3GENIChomozygous115366505