chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101553631215536313TC48INTERGENIChomozygous781403052
101553663515536636AG62INTERGENIChomozygous781403053
101553700115537002GT68INTERGENIChomozygous781403054
101553706815537069CG69INTERGENIChomozygous781403055
101553707615537077AG75INTERGENICpossibly homozygous781403056
101553733915537340GA88INTERGENICpossibly homozygous781403057
101553755115537552AT52INTERGENIChomozygous781403058
101553757415537575CG40INTERGENIChomozygous781403059
101553763915537640CT51INTERGENIChomozygous781403060
101553882215538823GA46INTERGENICpossibly homozygous781403061