chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108631468986314690CT34GENIChomozygous804096363
108631488886314889AG17GENIChomozygous804096364
108631736686317367GT30GENICpossibly homozygous804096365
108632007386320074GT13GENIChomozygous804096366
108632117686321177AG25GENIChomozygous804096367
108632166286321663GA23GENIChomozygous804096368
108632189886321899TC16GENIChomozygous804096369
108632223486322235CT24GENIChomozygous804096370
108632232886322329CT46GENIChomozygous804096371
108632233386322334AG45GENIChomozygous804096372
108633105086331051AG28GENIChomozygous804096373
108633257886332579GT41GENIChomozygous804096374
108633422186334222GA28GENIChomozygous804096375