chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218003133218003134CT16INTERGENIChomozygous61086672
1218003264218003265GA19INTERGENIChomozygous61086673
1218003342218003343GA4INTERGENIChomozygous61086674
1218003598218003599TC23INTERGENIChomozygous61086675
1218004135218004136TC22INTERGENIChomozygous61086676
1218004342218004343GT26INTERGENIChomozygous61086677
1218004405218004406GA26INTERGENIChomozygous61086678
1218005062218005063AG16INTERGENIChomozygous61086679
1218005237218005238AAT18INTERGENIChomozygous61086680
1218005724218005725AC28INTERGENIChomozygous61086681
1218005930218005931AG24INTERGENIChomozygous61086682
1218006127218006128TTAC4INTERGENICheterozygous61086683
1218006225218006226GA18INTERGENIChomozygous61086684
1218006311218006312CT30INTERGENIChomozygous61086685
1218006535218006536GA19INTERGENIChomozygous61086686
1218006570218006571TG12INTERGENIChomozygous61086687
1218006686218006687AT26INTERGENIChomozygous61086688
1218006134218006138ACAC----4INTERGENICheterozygous62355150