chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100453740100453741GA79GENIChomozygous117619632
9100454305100454306GA78GENIChomozygous117619634
9100454306100454307TA78GENIChomozygous117619636
9100455072100455073AC60GENIChomozygous117619638
9100455134100455135CT54GENIChomozygous117619640
9100457924100457924TGC59GENIChomozygous128737392
9100458959100458960GA62GENIChomozygous117619642
9100460269100460269TCCTTAGAACCGGCTTT36GENIChomozygous128737393
9100461545100461599CCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGC34GENIChomozygous128737394
9100462506100462507TA68GENIChomozygous117619644
9100463061100463062AG60GENIChomozygous117619646
9100463918100463919CT65GENIChomozygous117619648
9100465199100465200AG53GENIChomozygous117619650
9100465789100465790AT64GENIChomozygous117619652
9100466014100466015CT47GENIChomozygous117619654
9100466497100466498AG56GENIChomozygous117619656
9100466730100466731TC68GENIChomozygous117619658
9100468820100468821CT48GENIChomozygous117619660
9100469094100469095TC61GENIChomozygous117619662
9100469095100469096GT61GENIChomozygous117619664
9100469135100469136CT58GENIChomozygous117619666
9100470261100470262TC55GENIChomozygous117619668
9100470916100470917GA45GENIChomozygous117619670
9100471616100471617CT61GENICpossibly homozygous117619672
9100471780100471781CT46GENIChomozygous117619674
9100474008100474009GA56GENIChomozygous117619676
9100475377100475378GA47GENIChomozygous117400132
9100476729100476730GA88GENIChomozygous117619678
9100476874100476875TA46GENIChomozygous117619680
9100477784100477785TC59GENIChomozygous117619682
9100478119100478120TC59GENIChomozygous117619684
9100478906100478907TC57GENIChomozygous117619686
9100479484100479485AG71GENIChomozygous117619688