chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122219562922195630CT34GENIChomozygous115280631
122219619222196193AG34GENIChomozygous115280633
122219620322196204CT29GENIChomozygous115280635
122219646422196465AG29GENIChomozygous115280637
122219650722196508GA27GENIChomozygous115280639
122219668622196687CT31GENIChomozygous115280641
122219798522197986TC29GENICheterozygous118261188
122219806622198067GA30GENIChomozygous115280645
122219807322198074TC29GENIChomozygous115280647
122219855022198551CA25GENIChomozygous115280649
122219866722198668GT27GENIChomozygous115280651
122219891522198916GC19GENIChomozygous115445703
122219974822199749AG31GENIChomozygous118261190
122220041622200417AG20GENIChomozygous115280655
122220059622200597GA24GENIChomozygous115280657
122220153622201537AG25GENIChomozygous115280659
122220221322202214AC28GENIChomozygous115280661
122220229622202297GA26GENIChomozygous115280663
122220316022203161GA21GENIChomozygous115280665
122220332122203322TC27GENIChomozygous115280667
122220363522203636GA29GENIChomozygous115280669
122220365922203660CT29GENIChomozygous115280671
122220376122203762GA24GENIChomozygous115280673
122220382622203827AG26GENIChomozygous115280675
122220452822204529AG18GENIChomozygous115445705
122220482222204823CA2GENIChomozygous115691477
122220487022204871AC4GENIChomozygous118261196
122220556822205569TC13GENICpossibly homozygous118300554
122220560922205610AG12GENICpossibly homozygous118261198
122220656922206570GA15GENICpossibly homozygous115445707
122220772222207723GA13GENICpossibly homozygous118300556
122220816922208170TC24GENICheterozygous118331297
122220847522208476AT24GENIChomozygous115280683
122220907622209077CT21GENIChomozygous115366501
122220950622209507TC43GENIChomozygous115280687
122220990022209901CA29GENIChomozygous115280689
122221021722210218AG40GENIChomozygous115280691
122221068322210684AG33GENIChomozygous115366503
122220480622204807CA4GENIChomozygous115653493