chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32326105323261054AG5GENIChomozygous112224464
32326125323261254TC13GENIChomozygous125821930
32326319123263192CT15GENIChomozygous111506198
32326429123264292CT15GENIChomozygous111506200
32326446023264461CT20GENICpossibly homozygous111506201
32326475923264760TC23GENIChomozygous111506202
32326487323264874AC22GENIChomozygous111506203
32326537223265373AG12GENIChomozygous111506204
32326639023266391AG23GENIChomozygous111506205
32326714023267141GC13GENIChomozygous111506206
32326727523267276CT22GENIChomozygous111506207
32326735623267357TG24GENIChomozygous111506208
32326854423268545TC25GENIChomozygous111506211
32326862023268621GA20GENIChomozygous111506212
32327022623270227GT17GENIChomozygous111506214
32327157623271577AG12GENIChomozygous111506215