| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:153002643-153002838 | Common:3; Rare:70 | ||||
| chr6:158168205-158168393 | Common:2; Rare:66 | ||||
| chr6:158644710-158644919 | Common:2; Rare:82 | ||||
| chr6:159693148-159693587 | Common:6; Rare:129 | ||||
| chr6:159726995-159727162 | Rare:58 | ||||
| chr6:159789534-159789952 | Common:4; Rare:137 | ||||
| chr6:159790311-159790506 | Common:6; Rare:59 | ||||
| chr6:166342513-166342653 | Common:3; Rare:55 | ||||
| chr6:166999095-166999402 | Common:1; Rare:104 | ||||
| chr6:169751563-169751645 | Rare:32; Clinvar (benign):1 | ||||
| chr6:170554154-170554403 | Common:1; Rare:77 | ||||
| chr7:727246-727281 | Rare:13; Clinvar:1 | ||||
| chr7:1570018-1570142 | Common:1; Rare:41 | ||||
| chr7:2242171-2242247 | Common:2; Rare:47 | ||||
| chr7:2354063-2354111 | Rare:23 |