| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57744875-57745130 | Common:1; Rare:63 | ||||
| chr12:57745259-57745422 | Common:1; Rare:31 | ||||
| chr12:57751645-57751959 | Rare:70; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:57752064-57752730 | Common:2; Rare:161; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:57771773-57771882 | Rare:23 | ||||
| chr12:57772048-57772293 | Rare:85 | ||||
| chr12:57772492-57772696 | Common:3; Rare:38 | ||||
| chr12:57846374-57846523 | Rare:49 | ||||
| chr12:57846920-57847224 | Common:2; Rare:111 | ||||
| chr12:57941483-57941801 | Common:2; Rare:92 | ||||
| chr12:58920128-58920308 | Common:1; Rare:55 | ||||
| chr12:58920490-58920704 | Common:2; Rare:73 | ||||
| chr12:62260062-62260414 | Common:1; Rare:127 | ||||
| chr12:62466688-62466844 | Rare:54 | ||||
| chr12:63779749-63779881 | Common:2; Rare:45 |