chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3164041199164041200GT33GENICpossibly homozygous111806214
3164042509164042510AC25GENIChomozygous111806216
3164043898164043899GC36GENIChomozygous111806218
3164044410164044411CT15GENIChomozygous111806222
3164044501164044502GA28GENIChomozygous111806224
3164044511164044512CA29GENIChomozygous111806226
3164045672164045673TC24GENIChomozygous111806228
3164046514164046515AG33GENIChomozygous111806230
3164047970164047971AC22GENIChomozygous111806232
3164049231164049232CT18GENIChomozygous111806234