| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30754758-30755060 | Common:1; Rare:121 | ||||
| chr12:31073745-31073892 | Common:7; Rare:56 | ||||
| chr12:31324139-31324261 | Rare:31 | ||||
| chr12:31326118-31326435 | Common:4; Rare:111 | ||||
| chr12:31728984-31729277 | Common:1; Rare:94 | ||||
| chr12:31959269-31959488 | Common:2; Rare:73 | ||||
| chr12:38905567-38905670 | Common:3; Rare:28 | ||||
| chr12:39619785-39620091 | Common:1; Rare:51 | ||||
| chr12:40224722-40225013 | Common:5; Rare:65; Clinvar (benign):1 | ||||
| chr12:42238153-42238471 | Common:1; Rare:102 | ||||
| chr12:42325948-42326218 | Common:1; Rare:85 | ||||
| chr12:43758745-43759011 | Common:2; Rare:74; Clinvar:2 | ||||
| chr12:45215978-45216204 | Common:1; Rare:71 | ||||
| chr12:45990440-45990924 | Common:2; Rare:154 | ||||
| chr12:46268477-46268711 | Common:2; Rare:48 |