chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8107079200107079201GT14GENIChomozygous146889351
8107079614107079614C7GENICpossibly homozygous138263155
8107085544107085545GC17GENIChomozygous138409603
8107080379107080380TC18GENIChomozygous138409601
8107080922107080923CA16GENIChomozygous138409602
8107080592107080593GC18GENIChomozygous147280034
8107081011107081012CT20GENIChomozygous147280035
8107083852107083853GA22GENIChomozygous147280036
8107084225107084226CT11GENIChomozygous147280037
8107082679107082680A13GENICpossibly homozygous141017258
8107086707107086708AC22GENIChomozygous147280038
8107086961107086962GT24GENIChomozygous146889353
8107087677107087678GA15GENIChomozygous138409604