| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30695826-30696036 | Common:3; Rare:57 | ||||
| chr12:30754758-30755087 | Common:1; Rare:131 | ||||
| chr12:31073738-31073892 | Common:7; Rare:58 | ||||
| chr12:31324101-31324245 | Rare:36 | ||||
| chr12:31326041-31326475 | Common:4; Rare:139 | ||||
| chr12:31729010-31729320 | Common:1; Rare:96 | ||||
| chr12:31959156-31959179 | Rare:4 | ||||
| chr12:31959287-31959488 | Common:2; Rare:65 | ||||
| chr12:32485730-32486057 | Rare:55 | ||||
| chr12:32755455-32755520 | Rare:23; Clinvar (pathogenic):1 | ||||
| chr12:38905262-38905441 | Rare:47 | ||||
| chr12:38905491-38905766 | Common:4; Rare:79 | ||||
| chr12:38906175-38906534 | Common:2; Rare:71 | ||||
| chr12:38906564-38906623 | Rare:15 | ||||
| chr12:38906707-38906847 | Common:1; Rare:32 |