chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
179003406590034066TC43GENIChomozygous111141494
179003920690039207AG60GENICpossibly homozygous111370688
179004155290041553CT36GENIChomozygous111141496
179004613490046135AG49GENIChomozygous111141498
179005005790050058AT50GENIChomozygous111141500
179005273690052737AC48GENIChomozygous111225346
179005689690056897TC20GENIChomozygous111656962
179006082390060824AT82GENIChomozygous111141508
179006124690061247AG71GENIChomozygous111141510
179006129790061298CG68GENIChomozygous111141512
179006154190061542TG66GENIChomozygous111141513
179006199290061993TG56GENIChomozygous111141517
179006210290062103AG65GENIChomozygous111141519
179006358690063587GA66GENIChomozygous111370692
179006891490068915CG32GENIChomozygous119314627