chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13102755981102755982CG40GENICpossibly homozygous139365717
13102762801102762802C19GENICheterozygous139190332
13102775640102775641TC13GENICheterozygous403776309
13102775629102775630G38GENICheterozygous139190334
13102775629102775630GT38GENIChomozygous403347466
13102775640102775641T13GENICheterozygous403776308
13102792584102792584A25GENIChomozygous139190341