chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18063279880632798T12GENIChomozygous127397657
18063519980635201AC18GENICheterozygous130619274
18063580380635804AG12GENIChomozygous108140188
18063581580635817AA8GENIChomozygous127397658
18063582480635826AT8GENIChomozygous127397659
18063582780635828A8GENIChomozygous127397660
18063583280635840AACTAAAA7GENIChomozygous127397661
18063584480635844CTT8GENIChomozygous127397662
18063585380635853T9GENIChomozygous127397663
18063585780635857TC10GENIChomozygous127397664
18063586480635865C9GENIChomozygous127397665
18063591180635913AC10GENIChomozygous127397666
18063596480635965T17GENIChomozygous127397667
18063597980635979T22GENIChomozygous127397668
18063600980636010A29GENIChomozygous127397669
18063601480636015A29GENIChomozygous127397670
18063604680636047C30GENIChomozygous127397671
18063605680636057TA32GENIChomozygous108728967
18063605780636058AG31GENIChomozygous108728968
18063607780636078G27GENIChomozygous127397672
18063608580636086CT28GENIChomozygous108140189
18063610780636108AG27GENIChomozygous120481396
18063610780636107T26GENIChomozygous127397673
18063613780636138CG24GENIChomozygous108140190
18063615080636151C23GENIChomozygous127397674
18063615180636152GA24GENIChomozygous120481397
18063617280636173GT19GENIChomozygous108728969
18063617580636176CG19GENIChomozygous120481398
18063618180636181G18GENIChomozygous127397675
18063618880636188T19GENIChomozygous127397676
18063619580636195C20GENIChomozygous127397677
18063621780636218CA18GENIChomozygous108140191
18063628580636287CC20GENIChomozygous127397678
18063629080636291C22GENIChomozygous127397679
18064080280640802TA17GENIChomozygous127397680
18064083680640836GGGGCGTGGCTCAATGGTAGAGCCCCTGCCTAGAATCCCCCAGTGAGGGGCT13GENIChomozygous127397681
18064261880642618G23GENIChomozygous127397682
18064538580645385CCACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGAGGCTCTA5GENICheterozygous127397683
18066263680662639TAG6GENIChomozygous127397684