| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31074079-31074271 | Common:1; Rare:38 | ||||
| chr12:31324080-31324316 | Rare:53 | ||||
| chr12:31326091-31326439 | Common:4; Rare:120 | ||||
| chr12:31729012-31729352 | Common:1; Rare:102 | ||||
| chr12:31959262-31959490 | Common:2; Rare:73 | ||||
| chr12:32399807-32399932 | Common:1; Rare:38 | ||||
| chr12:32679091-32679403 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755878-32755985 | Rare:39 | ||||
| chr12:32896760-32896990 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905532-38905684 | Common:3; Rare:44 | ||||
| chr12:40224848-40225060 | Common:5; Rare:53; Clinvar (benign):1 | ||||
| chr12:42325971-42326214 | Common:1; Rare:78 | ||||
| chr12:43758749-43759016 | Common:2; Rare:75; Clinvar:2 | ||||
| chr12:43806213-43806385 | Common:2; Rare:56 | ||||
| chr12:45215982-45216184 | Common:1; Rare:66 |