| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53501174-53501352 | Rare:43 | ||||
| chr12:53501526-53501596 | Rare:16 | ||||
| chr12:53626333-53626520 | Common:3; Rare:49 | ||||
| chr12:53727424-53727719 | Rare:65 | ||||
| chr12:54188930-54189148 | Rare:49 | ||||
| chr12:54259517-54259655 | Rare:28 | ||||
| chr12:54300854-54301148 | Rare:55 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:54561182-54561495 | Common:1; Rare:48 | ||||
| chr12:54588404-54588694 | Rare:73 | ||||
| chr12:55707549-55707633 | Rare:32; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:55712056-55712537 | Common:8; Rare:104; Clinvar (benign):1 | ||||
| chr12:55715973-55716195 | Common:2; Rare:99 | ||||
| chr12:55728940-55729249 | Rare:64 | ||||
| chr12:55729661-55729819 | Rare:37 |