| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56725488-56725585 | Rare:24 | ||||
| chr12:56752303-56752457 | Rare:48 | ||||
| chr12:57111326-57111436 | Rare:25 | ||||
| chr12:57230010-57230221 | Rare:45 | ||||
| chr12:57533991-57534310 | Rare:86 | ||||
| chr12:57772087-57772251 | Rare:56 | ||||
| chr12:57772526-57772636 | Common:2; Rare:16 | ||||
| chr12:57846444-57846468 | Rare:8 | ||||
| chr12:57941360-57941708 | Common:3; Rare:102 | ||||
| chr12:58919496-58919612 | Rare:28 | ||||
| chr12:59595862-59596182 | Common:5; Rare:76 | ||||
| chr12:62260165-62260424 | Common:1; Rare:93 | ||||
| chr12:63780093-63780175 | Rare:39; Clinvar (pathogenic):1 | ||||
| chr12:64222242-64222372 | Rare:42 | ||||
| chr12:64404258-64404645 | Common:5; Rare:140 |