chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151552884151552885CT2GENICheterozygous56356457
5151553365151553366GA23GENICpossibly homozygous55925191
5151553517151553518GC7GENIChomozygous55925193
5151553519151553520CA6GENIChomozygous55925195
5151554049151554050AG7GENICpossibly homozygous55925197
5151554912151554913AC13GENIChomozygous55925199
5151555170151555171G-7GENICpossibly homozygous55796977
5151555323151555324CCT2GENICheterozygous55796978
5151555323151555324CCTT2GENICheterozygous55796979
5151556199151556200AAC7GENICpossibly homozygous55925201
5151556551151556552CT12GENICheterozygous55925203
5151556882151556883TC18GENIChomozygous55796982