chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3122130393122130394GC27GENIChomozygous111690083
3122130412122130413CT29GENIChomozygous111690084
3122130413122130414AG28GENIChomozygous111690085
3122137422122137423CT29GENIChomozygous111690086
3122140017122140018GA26GENIChomozygous111690087
3122143075122143076AG24GENIChomozygous111690088
3122141456122141456TGTGTGTGTGCACG20GENICpossibly homozygous127924920
3122148892122148893C21GENIChomozygous127924921
3122151120122151121T21GENIChomozygous127924922