chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221756431221756432TC13GENIChomozygous108545187
1221756674221756675CA5GENIChomozygous108545189
1221757118221757119CT16GENIChomozygous108545191
1221757432221757433TC13GENIChomozygous108545193
1221757607221757608TC21GENIChomozygous108545195
1221757932221757933AG9GENIChomozygous108545197
1221758933221758934TC15GENIChomozygous108545199
1221761353221761354GA20GENIChomozygous108545201
1221764125221764126CT9GENIChomozygous108545205
1221764698221764699AG17GENIChomozygous108545207
1221767667221767668CT3GENICheterozygous125535343
1221769439221769440AG18GENIChomozygous125309147
1221770903221770904CT16GENICheterozygous108545211
1221770929221770930AG12GENIChomozygous108545213