chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117909582117909583A-31GENICheterozygous754627164
1117909608117909609GT35GENIChomozygous645885523
1117909700117909701CCA13GENIChomozygous754627165
1117910380117910381GC30GENICpossibly homozygous645885524
1117910676117910677G-19GENICheterozygous754627166
1117910715117910716CG19GENICheterozygous645885525
1117910718117910719CT18GENICheterozygous645885526
1117910719117910720CT18GENICheterozygous645885527
1117910719117910720CA18GENICheterozygous645885528
1117910722117910723CG14GENIChomozygous645885529
1117910730117910731T-13GENICheterozygous754627167
1117910735117910736AG8GENIChomozygous645885530
1117910935117910936G-10GENICheterozygous754627168
1117911018117911019CCT36GENIChomozygous754627169