chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207866113207866114GT4GENICheterozygous61769917
2207867596207867597CT28GENICpossibly homozygous61769919
2207869284207869285GA9GENIChomozygous61769921
2207871200207871201AG11GENICpossibly homozygous59356626
2207871595207871596GGCCTGGCT2GENIChomozygous59356627
2207871908207871909CG19GENICpossibly homozygous61769923
2207872174207872175AG15GENICpossibly homozygous61769925
2207874239207874240CG13GENICheterozygous61769929