chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117684391117684392GA52GENICpossibly homozygous808103235
7117685548117685549CT54GENIChomozygous808103236
7117685747117685748AG45GENIChomozygous808103237
7117686227117686228GC44GENICpossibly homozygous808103238
7117686259117686260AG40GENIChomozygous808103239
7117686264117686265AT41GENIChomozygous808103240
7117686634117686635AG43GENIChomozygous808103241
7117687795117687796TC45GENIChomozygous808103242
7117688022117688023GA27GENIChomozygous808103243