| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45990419-45990973 | Common:3; Rare:177 | ||||
| chr12:46267310-46267475 | Rare:34 | ||||
| chr12:46268601-46268715 | Common:1; Rare:27 | ||||
| chr12:46269137-46269167 | Rare:8 | ||||
| chr12:46372685-46372956 | Rare:116 | ||||
| chr12:47705960-47706136 | Rare:72 | ||||
| chr12:47773114-47773266 | Rare:58 | ||||
| chr12:47813031-47813173 | Rare:33 | ||||
| chr12:47819864-47820128 | Common:2; Rare:63 | ||||
| chr12:48004453-48004594 | Common:2; Rare:22; Clinvar (benign):1 | ||||
| chr12:48004595-48004721 | Rare:27 | ||||
| chr12:48004725-48004864 | Rare:40 | ||||
| chr12:48105828-48105956 | Rare:33 | ||||
| chr12:48105979-48106218 | Common:2; Rare:80 | ||||
| chr12:48106277-48106419 | Rare:43 |