| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:24562352-24562507 | Common:1; Rare:40 | ||||
| chr12:24855912-24855972 | Common:1; Rare:11 | ||||
| chr12:24877440-24877564 | Common:1; Rare:23 | ||||
| chr12:24930158-24930217 | Rare:9 | ||||
| chr12:24936319-24936485 | Common:3; Rare:28 | ||||
| chr12:25209909-25210028 | Common:1; Rare:21; Clinvar (benign):4 | ||||
| chr12:25386017-25386380 | Common:4; Rare:130 | ||||
| chr12:25954841-25955104 | Common:1; Rare:38 | ||||
| chr12:25958115-25958239 | Common:1; Rare:26 | ||||
| chr12:25958244-25958283 | Rare:13 | ||||
| chr12:26126137-26126249 | Rare:29 | ||||
| chr12:26811641-26811931 | Common:7; Rare:49 | ||||
| chr12:27023665-27023765 | Common:1; Rare:15 | ||||
| chr12:27401265-27401538 | Rare:61 | ||||
| chr12:27532233-27532452 | Common:1; Rare:26 |