chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
179003406590034066TC43GENIChomozygous782836384
179003920690039207AG60GENICpossibly homozygous782836385
179004155290041553CT36GENIChomozygous782836386
179004613490046135AG49GENIChomozygous782836387
179005005790050058AT50GENIChomozygous782836388
179005273690052737AC48GENIChomozygous782836389
179005689690056897TC20GENIChomozygous782836390
179006082390060824AT82GENIChomozygous782836391
179006124690061247AG71GENIChomozygous782836392
179006129790061298CG68GENIChomozygous782836393
179006154190061542TG66GENIChomozygous782836394
179006199290061993TG56GENIChomozygous782836395
179006210290062103AG65GENIChomozygous782836396
179006358690063587GA66GENIChomozygous782836397
179006891490068915CG32GENIChomozygous782836398