chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1420204262020427CA49GENIChomozygous782079857
1420204372020438TC42GENIChomozygous782079858
1420211482021149AG45GENIChomozygous782079859
1420211762021177TC47GENIChomozygous782079860
1420214172021418AG34GENIChomozygous782079861
1420224522022453AG60GENIChomozygous782079862
1420226232022624AG60GENIChomozygous782079863
1420234352023436CT35GENIChomozygous782079864
1420235412023542GA53GENIChomozygous782079865
1420238482023849AG39GENIChomozygous782079866
1420241392024140AG36GENIChomozygous782079867
1420241602024161AG40GENIChomozygous782079868
1420244562024457CT54GENIChomozygous782079869
1420250422025043CT48GENIChomozygous782079870
1420250502025051GA45GENIChomozygous782079871
1420269902026991TC61GENIChomozygous782079872
1420272112027212AG67GENIChomozygous782079873
1420276632027664GA72GENICpossibly homozygous782079874
1420284712028472CT58GENICpossibly homozygous782079875
1420305142030515GA51GENIChomozygous782079876
1420310962031097CT48GENIChomozygous782079877
1420311712031172TC55GENIChomozygous782079878