chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144445624144445625CG21GENIChomozygous114037234
5144446204144446205GA27GENIChomozygous114650218
5144447075144447075T23GENIChomozygous128249972
5144447867144447868GA12GENIChomozygous114650220
5144450137144450138AC14GENIChomozygous114037235
5144454464144454469AAAAC11GENIChomozygous132844691
5144455102144455102A18GENICpossibly homozygous128249975
5144455153144455157GATC22GENIChomozygous134206299
5144455542144455543CT15GENIChomozygous114037239
5144456118144456118AAGGGAATAAC22GENIChomozygous128249977
5144456360144456482AAAAATTGTCAGATGTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAATCAAAAAAAAAAAAAAAAAAA10GENIChomozygous128249978
5144462132144462136AAAG15GENIChomozygous134206300
5144464288144464289GA17GENIChomozygous114037244
5144464635144464636GT17GENIChomozygous114037246
5144465347144465348TG20GENIChomozygous114037247
5144468970144468971CG15GENIChomozygous114650228
5144469352144469353T15GENIChomozygous128249981
5144469964144469965GA16GENIChomozygous114650232
5144470469144470470TC19GENIChomozygous114037250
5144471395144471396TC23GENIChomozygous114650234
5144472792144472793TC19GENIChomozygous114037251
5144472796144472797AG20GENIChomozygous114037252
5144472987144472988AG28GENIChomozygous114650236
5144473084144473085GA23GENIChomozygous114037253
5144475016144475017AC24GENIChomozygous114650240
5144475284144475285CT17GENIChomozygous114037257
5144475793144475794GA14GENIChomozygous114650242
5144476298144476299G16GENIChomozygous134206301
5144476958144476959GA18GENIChomozygous114037260
5144477069144477069C17GENIChomozygous128249982
5144477140144477141CT18GENIChomozygous114037261
5144477467144477468CA21GENIChomozygous114650244
5144477623144477624TG15GENIChomozygous114037262
5144478190144478191AT14GENIChomozygous114037264
5144479062144479063TC14GENIChomozygous114037265
5144461153144461161GTGTGTGC6GENIChomozygous134285125