chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2108518874108518875GGA11GENIChomozygous815575152
2108519302108519303TC9GENIChomozygous815575153
2108525901108525902GA17GENIChomozygous815575154
2108525977108525978G-18GENIChomozygous815575155
2108530591108530592CT15GENIChomozygous815575156
2108530793108530794AG21GENIChomozygous815575157
2108531342108531343CCT12GENICheterozygous815575158
2108534345108534346AG19GENIChomozygous815575159
2108535070108535071GA29GENIChomozygous815575160
2108535579108535580TC19GENIChomozygous815575161