chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12628876628877GT9GENIChomozygous786505079
12629151629152CT10GENIChomozygous786505080
12631942631943CA20GENIChomozygous786505081
12632987632988TC19GENIChomozygous786505082
12632993632994TA21GENIChomozygous786505083
12634650634651AG28GENIChomozygous786505084
12637190637191CA11GENIChomozygous786505085
12639307639308CT20GENIChomozygous786505086
12640764640765AG26GENICheterozygous786505087