chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135962811135962812G18GENIChomozygous128242680
5135963551135963560AAGTCGGGA9GENIChomozygous131650231
5135963921135963922AG19GENIChomozygous114018740
5135964210135964211CT13GENIChomozygous114442832
5135964264135964265AG15GENIChomozygous114018741
5135964548135964559TGATTCCCTGA11GENIChomozygous131650232
5135965311135965312AG17GENIChomozygous114018743
5135965873135965874CT12GENIChomozygous114442834
5135966183135966184AT13GENIChomozygous114018745
5135967576135967577CT1GENIChomozygous114018746
5135968347135968348TC21GENIChomozygous114018747
5135968788135968789CT17GENIChomozygous114018748
5135968885135968885AAGAGG17GENIChomozygous128242682
5135969112135969113AG32GENIChomozygous114018749
5135969913135969914TC12GENIChomozygous114018750
5135970528135970529AT15GENIChomozygous114018751
5135970722135970723GT27GENIChomozygous114018752
5135970913135970927TATCCCCCAAAATG15GENIChomozygous131650233
5135974288135974290CA14GENIChomozygous131650234
5135974794135974794CCGTGAGG10GENIChomozygous128242683
5135974978135974979AG23GENIChomozygous114018755
5135975795135975796GA18GENIChomozygous114442838
5135979688135979689TC2GENIChomozygous131657571
5135980081135980203CCAACCATTCTTTTTTTTTTTTAATTTTTTTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC3GENICheterozygous128242685
5135980506135980507GT23GENIChomozygous114442840
5135980528135980529A20GENIChomozygous131650235
5135980996135980997AG17GENIChomozygous114018760
5135982248135982249GT23GENICpossibly homozygous114442842
5135982627135982628AG16GENIChomozygous114018762
5135982678135982679AG17GENIChomozygous114018763
5135982688135982689AT16GENIChomozygous114018764
5135983623135983624GA12GENIChomozygous114442844