| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4649045-4649165 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr12:6200004-6200471 | Common:4; Rare:136 | ||||
| chr12:6375469-6375539 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6383999-6384250 | Common:1; Rare:53 | ||||
| chr12:6470672-6470814 | Rare:37 | ||||
| chr12:6493202-6493381 | Common:6; Rare:49 | ||||
| chr12:6493742-6494135 | Common:2; Rare:116 | ||||
| chr12:6534355-6534860 | Common:8; Rare:207 | ||||
| chr12:6568241-6568382 | Rare:54 | ||||
| chr12:6606357-6606556 | Common:3; Rare:84 | ||||
| chr12:6688897-6689089 | Rare:63 | ||||
| chr12:6689445-6689748 | Common:2; Rare:76 | ||||
| chr12:6723828-6724172 | Common:1; Rare:76 | ||||
| chr12:6724189-6724296 | Rare:23 | ||||
| chr12:6753060-6753196 | Common:4; Rare:54 |