| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57229637-57229814 | Common:1; Rare:80 | ||||
| chr12:57230051-57230431 | Rare:80 | ||||
| chr12:57430755-57431059 | Common:1; Rare:72 | ||||
| chr12:57454980-57455541 | Rare:99 | ||||
| chr12:57459737-57459921 | Common:3; Rare:45 | ||||
| chr12:57477857-57477951 | Rare:18 | ||||
| chr12:57488787-57489105 | Common:3; Rare:74; Clinvar (benign):2 | ||||
| chr12:57520415-57520727 | Common:2; Rare:89 | ||||
| chr12:57549939-57550110 | Rare:45 | ||||
| chr12:57591088-57591290 | Common:5; Rare:99 | ||||
| chr12:57604532-57604857 | Rare:57 | ||||
| chr12:57633139-57633286 | Rare:50 | ||||
| chr12:57716407-57716718 | Rare:88 | ||||
| chr12:57744827-57745135 | Common:1; Rare:78 | ||||
| chr12:57745267-57745434 | Common:1; Rare:27 |