| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57240493-57240705 | Rare:41 | ||||
| chr12:57430495-57430906 | Common:2; Rare:90 | ||||
| chr12:57430939-57431265 | Common:3; Rare:122 | ||||
| chr12:57454919-57455325 | Common:1; Rare:78 | ||||
| chr12:57487835-57488164 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:57488519-57488610 | Rare:21 | ||||
| chr12:57488787-57489093 | Common:3; Rare:68; Clinvar (benign):2 | ||||
| chr12:57519975-57520032 | Rare:9 | ||||
| chr12:57520416-57521008 | Common:4; Rare:163 | ||||
| chr12:57521704-57521826 | Rare:23 | ||||
| chr12:57522089-57522258 | Rare:33 | ||||
| chr12:57522415-57522760 | Common:1; Rare:107 | ||||
| chr12:57522799-57522907 | Rare:30 | ||||
| chr12:57523174-57523292 | Rare:25 | ||||
| chr12:57523540-57523563 | Rare:4 |