chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15749247257492473TG32GENIChomozygous61870871
15750389157503892TC23GENIChomozygous61424555
15750400357504004AAT27GENICpossibly homozygous61424556
15750401657504018TT--19GENIChomozygous61870872
15750568957505693ACAC----13GENICheterozygous61292867
15750569157505693AC--13GENICpossibly homozygous61292869
15750607057506071CT6GENIChomozygous60714610
15750607757506078CG5GENIChomozygous60714611
15750681957506820GC46GENIChomozygous61870873
15750848857508489CT32GENIChomozygous61870874
15750882857508829TC28GENIChomozygous61424569