chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139273740139273741GA62GENIChomozygous115936621
7139274242139274243CT42GENIChomozygous115936622
7139274400139274401GC28GENIChomozygous115936623
7139274911139274912AG68GENIChomozygous115936624
7139275574139275575GA48GENICpossibly homozygous115936625
7139275715139275728AGCAGGTAGGGAA48GENIChomozygous128528515
7139275810139275811TC75GENICpossibly homozygous115936626
7139275850139275851TC76GENICpossibly homozygous115936627
7139276249139276250CT58GENIChomozygous115936628
7139277129139277130CT36GENIChomozygous115936629
7139278207139278208TG55GENICpossibly homozygous115936630
7139278475139278476GA52GENIChomozygous115936631
7139278594139278595CG56GENIChomozygous115936632
7139279240139279241GA52GENIChomozygous115936633