chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152455208152455209AC4GENIChomozygous119455011
4152459832152459833TA23GENIChomozygous112888200
4152467575152467576AT12GENIChomozygous113397517
4152467609152467610TC11GENIChomozygous112888201
4152474876152474877GA13GENIChomozygous113397519
4152475082152475083TC20GENIChomozygous112888204
4152479028152479029TA21GENIChomozygous113397521
4152482331152482332AG19GENIChomozygous112888208
4152500394152500395GT28GENIChomozygous113397525
4152503264152503265TC17GENIChomozygous112888214
4152505138152505139AG22GENIChomozygous112888216
4152510554152510555GA22GENIChomozygous112888217
4152512788152512789AG20GENIChomozygous112888219
4152518088152518089AG27GENIChomozygous112888220
4152519838152519839TC17GENIChomozygous112888222
4152535178152535179AT11GENICpossibly homozygous113244662
4152556947152556948CT10GENICpossibly homozygous113397531
4152564008152564009AC36GENIChomozygous112888240
4152566824152566825GT8GENIChomozygous112888241
4152567018152567019GA13GENIChomozygous112888242
4152573535152573536TG22GENIChomozygous113397533
4152576811152576812TC19GENIChomozygous113397535