chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140311230140311231GC47GENIChomozygous115938467
7140312679140312680CT37GENIChomozygous115938468
7140313280140313281TC48GENIChomozygous115938469
7140314253140314254AG18GENIChomozygous115938470
7140314891140314892CA73GENICpossibly homozygous115938471
7140315505140315506AG28GENIChomozygous115938472
7140315510140315511C25GENIChomozygous128528981
7140317099140317100TC54GENIChomozygous115938473
7140317477140317478TG53GENIChomozygous115938474
7140317761140317762GA55GENIChomozygous115938475
7140318266140318267TA51GENIChomozygous115938476
7140318764140318765TC29GENIChomozygous115938477
7140318936140318937TG36GENIChomozygous115938478
7140319563140319564CT42GENICpossibly homozygous115938479
7140320290140320291GA47GENIChomozygous115938480
7140320861140320862GA43GENIChomozygous115938481
7140320871140320871ACACACACACATCT41GENIChomozygous128528982
7140321816140321817C52GENIChomozygous128528983
7140322568140322569TA50GENIChomozygous115938482