chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151514195151514196CT5GENIChomozygous121896727
3151519404151519405TC20GENICpossibly homozygous112041862
3151519994151519995GC16GENIChomozygous111777676
3151528785151528786AG17GENIChomozygous111777692
3151530256151530257CT15GENIChomozygous111777694
3151531761151531762TC18GENIChomozygous111777696
3151535190151535191AG13GENIChomozygous111777698
3151541015151541016AG16GENIChomozygous111777700
3151543171151543172AG17GENIChomozygous111777702