chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214124348214124349AG29GENIChomozygous778740663
1214124410214124411CA24GENIChomozygous778740664
1214127012214127013GA52GENICheterozygous778740665
1214127053214127054GA45GENICpossibly homozygous778740666
1214127433214127434TC27GENICpossibly homozygous778740667
1214129031214129032TC56GENIChomozygous778740668
1214130226214130227GA53GENIChomozygous778740669
1214131357214131358AG50GENIChomozygous778740670
1214132380214132381AG44GENIChomozygous778740671
1214132530214132531CT56GENICpossibly homozygous778740672
1214137707214137708CG45GENICheterozygous778740673
1214138871214138872GA56GENIChomozygous778740674
1214140632214140633CT71GENIChomozygous778740675
1214140827214140828GT50GENIChomozygous778740676
1214140994214140995GT53GENICpossibly homozygous778740677
1214141343214141344AG53GENIChomozygous778740678
1214143187214143188CT56GENIChomozygous778740679
1214143347214143348AG51GENIChomozygous778740680
1214144102214144103GA64GENIChomozygous778740681
1214146027214146028TC51GENIChomozygous778740682
1214147016214147017CT52GENIChomozygous778740683