chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15749247257492473TG27GENIChomozygous61870871
15750389157503892TC12GENIChomozygous61424555
15750400357504004AAT19GENIChomozygous61424556
15750401657504018TT--9GENIChomozygous61870872
15750568957505693ACAC----14GENICheterozygous61292867
15750569157505693AC--14GENICpossibly homozygous61292869
15750607057506071CT5GENIChomozygous60714610
15750607757506078CG4GENIChomozygous60714611
15750681957506820GC9GENIChomozygous61870873
15750848857508489CT17GENIChomozygous61870874
15750882857508829TC17GENIChomozygous61424569