| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7109105-7109219 | Rare:38 | ||||
| chr12:7109222-7109397 | Rare:45 | ||||
| chr12:7155583-7155958 | Common:1; Rare:59 | ||||
| chr12:7189519-7189958 | Common:6; Rare:148; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:8032553-8032766 | Common:4; Rare:70 | ||||
| chr12:8697772-8698147 | Common:3; Rare:134 | ||||
| chr12:8949574-8950107 | Common:4; Rare:127 | ||||
| chr12:9079788-9080008 | Rare:42 | ||||
| chr12:9080093-9080327 | Rare:54 | ||||
| chr12:9089902-9090175 | Common:3; Rare:59 | ||||
| chr12:9106246-9106483 | Common:2; Rare:59 | ||||
| chr12:9115839-9116020 | Common:3; Rare:43 | ||||
| chr12:9760893-9761003 | Rare:14 | ||||
| chr12:9869347-9869494 | Common:1; Rare:24 | ||||
| chr12:10613528-10613645 | Rare:49 |