chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218003133218003134CT8INTERGENIChomozygous61086672
1218003264218003265GA23INTERGENICpossibly homozygous61086673
1218003342218003343GA7INTERGENICpossibly homozygous61086674
1218003598218003599TC20INTERGENIChomozygous61086675
1218004135218004136TC24INTERGENICpossibly homozygous61086676
1218004342218004343GT16INTERGENIChomozygous61086677
1218004405218004406GA14INTERGENIChomozygous61086678
1218005062218005063AG5INTERGENIChomozygous61086679
1218005724218005725AC15INTERGENIChomozygous61086681
1218005930218005931AG24INTERGENIChomozygous61086682
1218006225218006226GA22INTERGENIChomozygous61086684
1218006311218006312CT22INTERGENICpossibly homozygous61086685
1218006535218006536GA24INTERGENICheterozygous61086686
1218006570218006571TG16INTERGENICheterozygous61086687
1218006686218006687AT16INTERGENIChomozygous61086688