chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143793643143793644TC19GENIChomozygous125369211
1143794192143794193CT17GENIChomozygous125369212
1143794667143794668AC15GENIChomozygous108938463
1143795390143795391CT11GENIChomozygous125369213
1143795861143795862CT9GENIChomozygous125369214
1143796457143796458AG16GENIChomozygous125369215
1143796669143796670AC19GENIChomozygous125291417
1143797976143797977GA10GENIChomozygous125369216
1143798230143798231GT18GENIChomozygous125291419
1143800478143800479CT14GENIChomozygous125369217
1143801346143801347CT7GENIChomozygous125369218
1143801983143801984GA15GENIChomozygous125291420
1143802131143802132AG16GENIChomozygous125291422
1143802224143802225CT7GENIChomozygous125369219
1143802609143802610CG12GENIChomozygous125291423
1143805378143805379TC12GENIChomozygous108267121
1143803988143803989GA10GENIChomozygous108267117
1143805665143805666GA22GENIChomozygous109050646
1143806715143806716AG19GENIChomozygous108267125
1143806970143806971AG18GENIChomozygous108267127
1143807352143807353TC16GENIChomozygous108267129
1143808237143808238TC28GENIChomozygous108267131
1143810993143810994CT22GENIChomozygous109050650
1143811520143811521AG13GENIChomozygous108267137
1143814081143814082AG3GENICheterozygous125369220
1143814763143814764TA8GENIChomozygous109050652
1143815851143815852CA15GENIChomozygous108267143
1143805751143805752GA18GENICpossibly homozygous109328680
1143809249143809250GA11GENIChomozygous109328682
1143814892143814893GT14GENIChomozygous109328684
1143815860143815861CT14GENIChomozygous109328686