chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159872362698723627GT29GENIChomozygous112612405
159873797198737972AG66GENIChomozygous112612407
159874160598741606GA48GENIChomozygous112612409
159874161598741616GA50GENICpossibly homozygous112612411
159874636598746366TG50GENIChomozygous112612413
159875211098752111CT60GENIChomozygous112612415
159875326298753263CT51GENIChomozygous112612417
159875445698754457GA38GENIChomozygous112612419
159875599998756000AG34GENIChomozygous112612421
159875757098757571AG48GENICpossibly homozygous112612423
159875969998759700CG41GENICheterozygous118932437
159873544898735449GA52GENIChomozygous112826154
159873828698738287TC41GENICpossibly homozygous112826156