chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102773520102773521AG19GENICpossibly homozygous61486894
1102775846102775847CG22GENICheterozygous60780098
1102776685102776686C-16GENIChomozygous61486895
1102777665102777666TC24GENIChomozygous61486896
1102778266102778267C-15GENIChomozygous61486897
1102778709102778710GA24GENIChomozygous61486898
1102778922102778923CT21GENIChomozygous61486899
1102779087102779088TC16GENIChomozygous61486900