Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:152983009-152983281 | Common:2; Rare:82 | ||||
chr6:158168210-158168388 | Common:2; Rare:63 | ||||
chr6:158644710-158645022 | Common:2; Rare:101 | ||||
chr6:159726972-159727175 | Rare:67 | ||||
chr6:159789553-159789984 | Common:4; Rare:148 | ||||
chr6:166342513-166342648 | Common:3; Rare:52 | ||||
chr6:166999081-166999403 | Common:1; Rare:110 | ||||
chr7:727246-727281 | Rare:13; Clinvar:1 | ||||
chr7:1570018-1570094 | Common:1; Rare:25 | ||||
chr7:2242178-2242251 | Common:2; Rare:45 | ||||
chr7:4775523-4775634 | Common:4; Rare:45 | ||||
chr7:6009030-6009355 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):14 | ||||
chr7:17940467-17940574 | Common:1; Rare:43 | ||||
chr7:23105642-23105813 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
chr7:23531971-23532141 | Common:1; Rare:66 |