| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6536491-6536788 | Rare:98 | ||||
| chr12:6568241-6568382 | Rare:54 | ||||
| chr12:6688887-6689233 | Rare:107 | ||||
| chr12:6723969-6724172 | Rare:53 | ||||
| chr12:6851227-6851461 | Rare:56 | ||||
| chr12:6851890-6852182 | Rare:75 | ||||
| chr12:6867355-6867594 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873291-6873546 | Common:1; Rare:75 | ||||
| chr12:6914459-6914603 | Rare:42 | ||||
| chr12:6970545-6970977 | Common:4; Rare:138; Clinvar (benign):1 | ||||
| chr12:7108497-7108671 | Common:1; Rare:48 | ||||
| chr12:7189563-7189727 | Rare:62; Clinvar:4 | ||||
| chr12:8032590-8032793 | Rare:71 | ||||
| chr12:8914374-8914714 | Common:6; Rare:99 | ||||
| chr12:9869316-9869445 | Common:1; Rare:19 |