| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7130268-7130440 | Common:4; Rare:48 | ||||
| chr12:7502716-7502785 | Rare:16 | ||||
| chr12:7503643-7503830 | Rare:39 | ||||
| chr12:7503833-7503868 | Common:1; Rare:3 | ||||
| chr12:8032590-8032774 | Rare:65 | ||||
| chr12:8949951-8950099 | Common:1; Rare:43 | ||||
| chr12:9079618-9080179 | Common:1; Rare:133; Clinvar (benign):1 | ||||
| chr12:9115762-9116313 | Common:3; Rare:118 | ||||
| chr12:9760893-9761027 | Rare:19 | ||||
| chr12:10613449-10613763 | Common:2; Rare:113 | ||||
| chr12:11170987-11171272 | Common:3; Rare:82 | ||||
| chr12:11171567-11171848 | Common:8; Rare:82 | ||||
| chr12:12356981-12357204 | Common:4; Rare:111 | ||||
| chr12:12560839-12561279 | Common:5; Rare:97 | ||||
| chr12:13000037-13000476 | Common:2; Rare:137 |