chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31735694917356950CT15GENIChomozygous57176637
31735728117357282TC8GENIChomozygous57176639
31735764517357646TC11GENIChomozygous57176641
31735764617357647GA10GENIChomozygous57176643
31735769517357696GA8GENIChomozygous57176645
31735777017357771CT11GENIChomozygous57176647
31735791717357918CT19GENIChomozygous57176649
31735791817357919AG19GENIChomozygous57176651
31735793317357934TC20GENIChomozygous57176653
31735795917357960TC15GENIChomozygous57176655
31735799617357997AG12GENIChomozygous57176657
31735822617358227CA18GENIChomozygous57176659
31735825417358255GA28GENIChomozygous57176661
31735827317358274GA24GENIChomozygous57176663
31735839717358398CT10GENIChomozygous57176665
31735851217358513TC17GENIChomozygous57176667
31735856617358567TC23GENIChomozygous57176669
31735962417359625GA20GENIChomozygous57176671
31735963517359636GA23GENIChomozygous57176673
31736033617360337GA14GENIChomozygous57176675
31736163217361633CT5GENIChomozygous57176683
31736173517361736GT15GENIChomozygous57176685
31736177717361778TA16GENIChomozygous57176687
31736190617361907CT7GENIChomozygous57176689
31736217717362178TG23GENIChomozygous57176691
31736226917362270CT20GENIChomozygous57176693
31736268017362681AG22GENIChomozygous57176695
31736300617363016ACCAGCCCCG----------2GENICheterozygous57176697
31736315317363154AG4GENIChomozygous57176699
31736315517363156AAGGG2GENICheterozygous57176701
31736315517363156AAGGGG2GENICheterozygous59782987
31736330717363308TG6GENIChomozygous57176703
31736428117364282TG5GENIChomozygous57176705
31736512717365128GA9GENIChomozygous57176707