chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105541260155412602CA14INTERGENIChomozygous51889807
105541316355413164CG7INTERGENIChomozygous51889810
105541336355413364TTA11INTERGENICpossibly homozygous51889813
105541402455414025AG17INTERGENICpossibly homozygous51889816
105541456755414568CCA2INTERGENICheterozygous51889819
105541459255414601AAAAAAACA---------1INTERGENIChomozygous51889825
105541462255414623AC2INTERGENIChomozygous51889829
105541471755414718TC5INTERGENIChomozygous51652871
105541561855415619AT11INTERGENIChomozygous51889832
105541612855416129CCT3INTERGENICheterozygous51889838
105541663355416634TC11INTERGENIChomozygous51889841
105541784255417843GA18INTERGENICpossibly homozygous51889850
105541571855415719TC23INTERGENIChomozygous51459560
105542136055421361GGTT2GENICheterozygous51459568
105542178355421784GA14GENIChomozygous51889862
105542222655422227G-7GENICpossibly homozygous51889864
105542299155422992AC29INTERGENICpossibly homozygous51652883
105542339155423405AAAAAAGAAAAAAG--------------1INTERGENIChomozygous51889867
105542363955423640CT13INTERGENIChomozygous51889869
105542371655423717A-2INTERGENIChomozygous51889872
105542663455426635GA5GENIChomozygous51889875
105542388955423890A-2INTERGENICheterozygous51459571
105542704055427041AG19GENICpossibly homozygous51459574
105543135855431359CT17GENICpossibly homozygous51889878
105543405055434051TC7GENICpossibly homozygous51889883
105543455155434552TC4GENICheterozygous51459577
105543975055439751CT12GENIChomozygous51889886
105544122855441229CT25INTERGENICpossibly homozygous51652909
105544282455442834CTTCCCTTCC----------2INTERGENICheterozygous52377320
105544648155446482TC13INTERGENIChomozygous51459589
105544676055446761GA15INTERGENICpossibly homozygous51889902
105544860355448604CT5GENIChomozygous51459591
105544874255448743GT11GENICpossibly homozygous51889905
105544986855449869CT15GENIChomozygous51889908
105545344655453447TG7GENIChomozygous51889916
105545539055455391GC18GENICheterozygous51889919
105545574455455745CT16GENIChomozygous51889922