chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1104477431104477432GT21GENIChomozygous939986264
1104477450104477451GA21GENIChomozygous939986265
1104477451104477452AC21GENIChomozygous939986266
1104478304104478305CT26GENIChomozygous939986267
1104478470104478471GA42GENIChomozygous939986268
1104478570104478571GA36GENIChomozygous939986269
1104478785104478786AG34GENIChomozygous939986270
1104478921104478922TC27GENIChomozygous939986271
1104479048104479049GC39GENIChomozygous939986272
1104479079104479080GA37GENIChomozygous939986273
1104479358104479359TC37GENIChomozygous939986274
1104480826104480827AC24GENIChomozygous939986275
1104480929104480930AG31GENIChomozygous939986276
1104481234104481235AG34GENIChomozygous939986277