| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48716698-48717008 | Common:4; Rare:94 | ||||
| chr12:49018741-49018851 | Rare:51 | ||||
| chr12:49131341-49131621 | Common:2; Rare:107 | ||||
| chr12:49188998-49189171 | Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265083 | Common:4; Rare:107 | ||||
| chr12:49367226-49367539 | Common:1; Rare:86 | ||||
| chr12:49568110-49568278 | Common:2; Rare:50 | ||||
| chr12:49741391-49741593 | Rare:61 | ||||
| chr12:50085313-50085355 | Rare:7 | ||||
| chr12:50283452-50283632 | Rare:53 | ||||
| chr12:50763927-50764117 | Common:1; Rare:53 | ||||
| chr12:51048119-51048351 | Common:1; Rare:78 | ||||
| chr12:51238688-51238899 | Common:3; Rare:91 | ||||
| chr12:51270282-51270351 | Common:2; Rare:18 | ||||
| chr12:51391613-51391736 | Common:1; Rare:39 |