chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138972601389726014GA50GENIChomozygous782036360
138972624089726241TC44GENIChomozygous782036361
138972625889726259GA41GENIChomozygous782036362
138972660189726602CT50GENIChomozygous782036363
138972828389728284GA81GENICpossibly homozygous782036364
138972852489728525AG44GENIChomozygous782036365
138972910389729104GA54GENIChomozygous782036366
138973020289730203CT53GENIChomozygous782036367
138973099689730997GT30GENIChomozygous782036368
138973118789731188GC17GENICpossibly homozygous782036369
138973119989731200AT26GENICheterozygous782036370
138973120389731204TC24GENICheterozygous782036371
138973121489731215GT31GENICpossibly homozygous782036372
138973844189738442CG55GENICpossibly homozygous782036373
138973876889738769GT56GENIChomozygous782036374
138973972489739725GT30GENIChomozygous782036375
138974087489740875TC70GENIChomozygous782036376
138974098189740982TG56GENIChomozygous782036377
138974265889742659AG48GENICpossibly homozygous782036378