chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218003133218003134CT16INTERGENIChomozygous61086672
1218003264218003265GA30INTERGENIChomozygous61086673
1218003342218003343GA32INTERGENIChomozygous61086674
1218003598218003599TC35INTERGENIChomozygous61086675
1218004135218004136TC28INTERGENIChomozygous61086676
1218004342218004343GT32INTERGENIChomozygous61086677
1218004405218004406GA22INTERGENICpossibly homozygous61086678
1218005062218005063AG21INTERGENIChomozygous61086679
1218005237218005238AAT24INTERGENIChomozygous61086680
1218005724218005725AC32INTERGENIChomozygous61086681
1218005930218005931AG22INTERGENIChomozygous61086682
1218006127218006128TTAC5INTERGENICheterozygous61086683
1218006225218006226GA29INTERGENIChomozygous61086684
1218006311218006312CT19INTERGENIChomozygous61086685
1218006535218006536GA20INTERGENIChomozygous61086686
1218006570218006571TG24INTERGENIChomozygous61086687
1218006686218006687AT20INTERGENIChomozygous61086688