chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144444422144444422A21GENICpossibly homozygous132844690
5144446204144446205GA23GENIChomozygous114650218
5144447867144447868GA12GENIChomozygous114650220
5144445624144445625CG15GENIChomozygous114037234
5144450137144450138AC13GENIChomozygous114037235
5144447075144447075T15GENIChomozygous128249972
5144454464144454469AAAAC16GENIChomozygous132844691
5144455102144455102A12GENIChomozygous128249975
5144455542144455543CT13GENIChomozygous114037239
5144456118144456118AAGGGAATAAC15GENIChomozygous128249977
5144456187144456188CG14GENIChomozygous114037240
5144456252144456269TACTATACCTCAATGTC14GENIChomozygous132844692
5144456360144456482AAAAATTGTCAGATGTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAATCAAAAAAAAAAAAAAAAAAA7GENICheterozygous128249978
5144461298144461306TTGTTTGT13GENIChomozygous132844693
5144461574144461575TC21GENIChomozygous114037243
5144464288144464289GA11GENIChomozygous114037244
5144464599144464600CT13GENIChomozygous119018031
5144455604144455605GA11GENIChomozygous119018027
5144458656144458657CT19GENIChomozygous119018028
5144459508144459509CT22GENIChomozygous119018029
5144462425144462426CT27GENIChomozygous119018030
5144464635144464636GT12GENIChomozygous114037246
5144465543144465544GC20GENIChomozygous119018032
5144469352144469353T13GENICpossibly homozygous128249981
5144469964144469965GA9GENIChomozygous114650232
5144470469144470470TC20GENIChomozygous114037250
5144473015144473016GA20GENIChomozygous119018033
5144473084144473085GA13GENIChomozygous114037253