| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103929199-103929344 | Rare:27 | ||||
| chr12:103929408-103929577 | Common:2; Rare:56 | ||||
| chr12:103931238-103931268 | Rare:4 | ||||
| chr12:104045266-104045450 | Common:1; Rare:38 | ||||
| chr12:104276295-104276392 | Rare:16 | ||||
| chr12:104457512-104457679 | Rare:38 | ||||
| chr12:104458416-104458664 | Rare:55 | ||||
| chr12:104458995-104459372 | Common:3; Rare:61 | ||||
| chr12:104463026-104463219 | Common:2; Rare:32 | ||||
| chr12:104473255-104473343 | Rare:9 | ||||
| chr12:104473417-104473572 | Rare:18 | ||||
| chr12:104478502-104478680 | Common:2; Rare:26 | ||||
| chr12:104487347-104487467 | Common:2; Rare:17 | ||||
| chr12:104490981-104491201 | Common:4; Rare:32 | ||||
| chr12:104520681-104520813 | Rare:21 |