| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723830-6724109 | Common:1; Rare:56 | ||||
| chr12:6851239-6851346 | Rare:25 | ||||
| chr12:6851879-6852174 | Rare:78 | ||||
| chr12:6873330-6873541 | Common:1; Rare:58 | ||||
| chr12:6970510-6970964 | Common:4; Rare:139; Clinvar (benign):1 | ||||
| chr12:7018474-7018584 | Common:1; Rare:26 | ||||
| chr12:10172113-10172261 | Rare:36 | ||||
| chr12:10613515-10613666 | Common:1; Rare:61 | ||||
| chr12:11171571-11171705 | Common:2; Rare:47 | ||||
| chr12:12357004-12357137 | Common:1; Rare:69 | ||||
| chr12:12611765-12611936 | Common:2; Rare:53 | ||||
| chr12:12891289-12891567 | Common:1; Rare:56 | ||||
| chr12:13000196-13000447 | Common:1; Rare:83 | ||||
| chr12:14803439-14803715 | Common:1; Rare:72 | ||||
| chr12:15882319-15882631 | Common:1; Rare:83 |