chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15972161759721618TC67GENIChomozygous108116272
15972246859722469GA69GENICpossibly homozygous108116273
15972255559722556CA53GENIChomozygous108116274
15972528659725287TG66GENIChomozygous108116275
15972672759726728GT70GENIChomozygous108116276
15972680459726805TC67GENIChomozygous108116277
15972696159726962CT9GENICpossibly homozygous108116278
15972710759727108AT43GENIChomozygous108116279
15972740059727401AG42GENIChomozygous108116280
15972742759727428AT40GENIChomozygous108116281
15972792259727923TC39GENIChomozygous108116282
15972812359728124GC65GENIChomozygous108116283
15972900259729003GA45GENIChomozygous108116284
15972989459729895CT39GENICheterozygous108116285
15973089959730900AC69GENIChomozygous108116286