chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139273740139273741GA6GENIChomozygous115936621
7139274242139274243CT11GENIChomozygous115936622
7139274400139274401GC11GENIChomozygous115936623
7139274911139274912AG28GENICpossibly homozygous115936624
7139275574139275575GA14GENIChomozygous115936625
7139275810139275811TC13GENIChomozygous115936626
7139275850139275851TC17GENIChomozygous115936627
7139276249139276250CT14GENIChomozygous115936628
7139277129139277130CT9GENIChomozygous115936629
7139278207139278208TG18GENIChomozygous115936630
7139278475139278476GA27GENIChomozygous115936631
7139278594139278595CG23GENIChomozygous115936632
7139279240139279241GA19GENIChomozygous115936633