chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265506921265506922CT28GENIChomozygous108637134
1265507749265507750TG24GENIChomozygous108637135
1265510327265510328AC27GENIChomozygous108637136
1265510999265511000TC31GENIChomozygous108637138
1265512099265512100CT46GENIChomozygous108637139
1265512411265512412TC52GENIChomozygous108637140
1265513478265513479TC43GENIChomozygous108637141
1265514233265514234GA32GENIChomozygous108637142
1265516163265516164AC27GENIChomozygous108637143
1265517331265517332GA47GENIChomozygous108637144
1265519549265519550GA12GENIChomozygous108637145
1265529410265529411TC41GENIChomozygous108637148
1265529578265529579CT32GENIChomozygous108637149
1265530494265530495TC32GENIChomozygous108637150
1265530503265530504CG30GENIChomozygous108637151
1265530772265530773CT39GENIChomozygous108637152