| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32747328-32747464 | Rare:51; Clinvar:1 | ||||
| chr12:32755041-32755278 | Rare:71; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr12:39309264-39309516 | Common:1; Rare:39 | ||||
| chr12:39333917-39334178 | Rare:37 | ||||
| chr12:40037352-40037623 | Rare:40 | ||||
| chr12:41932462-41932729 | Common:3; Rare:68 | ||||
| chr12:42216561-42216781 | Common:1; Rare:29 | ||||
| chr12:42223701-42223962 | Common:1; Rare:40 | ||||
| chr12:42313730-42313895 | Common:1; Rare:45 | ||||
| chr12:42357064-42357226 | Common:1; Rare:31 | ||||
| chr12:42409179-42409198 | Rare:5 | ||||
| chr12:42451078-42451359 | Common:6; Rare:60 | ||||
| chr12:42453351-42453544 | Rare:38 | ||||
| chr12:42453701-42453871 | Rare:33 | ||||
| chr12:42460649-42460722 | Rare:15; Clinvar:1; Clinvar (benign):1 |