chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18063580380635804AG19GENIChomozygous108140188
18063581580635817AA16GENIChomozygous127397658
18063582480635826AT15GENIChomozygous127397659
18063582780635828A15GENIChomozygous127397660
18063583280635840AACTAAAA15GENIChomozygous127397661
18063584480635844CTT14GENIChomozygous127397662
18063585380635853T12GENIChomozygous127397663
18063585780635857TC11GENIChomozygous127397664
18063586480635865C10GENIChomozygous127397665
18063591180635913AC12GENIChomozygous127397666
18063596480635965T14GENIChomozygous127397667
18063597980635979T14GENIChomozygous127397668
18063600980636010A19GENIChomozygous127397669
18063601480636015A20GENIChomozygous127397670
18063604680636047C22GENIChomozygous127397671
18063607780636078G26GENIChomozygous127397672
18063608580636086CT27GENIChomozygous108140189
18063610780636108AG26GENIChomozygous120481396
18063610780636107T26GENIChomozygous127397673
18063613780636138CG26GENIChomozygous108140190
18063615080636151C28GENIChomozygous127397674
18063615180636152GA28GENIChomozygous120481397
18063617580636176CG25GENIChomozygous120481398
18063618180636181G25GENIChomozygous127397675
18063618880636188T25GENIChomozygous127397676
18063619580636195C27GENIChomozygous127397677
18063621780636218CA27GENIChomozygous108140191
18063628580636287CC22GENIChomozygous127397678
18063629080636291C21GENIChomozygous127397679
18064080280640802TA21GENIChomozygous127397680
18064083680640836GGGGCGTGGCTCAATGGTAGAGCCCCTGCCTAGAATCCCCCAGTGAGGGGCT16GENIChomozygous127397681
18064261880642618G25GENIChomozygous127397682
18063605680636057TA24GENIChomozygous108728967
18063605780636058AG23GENIChomozygous108728968
18063617280636173GT26GENIChomozygous108728969
18064538580645385CCACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGAGGCTCTA6GENIChomozygous127397683
18066263680662639TAG9GENIChomozygous127397684