| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905919-38906018 | Rare:26 | ||||
| chr12:38906151-38906207 | Rare:11 | ||||
| chr12:38906573-38907032 | Common:2; Rare:92 | ||||
| chr12:39442357-39442619 | Rare:46 | ||||
| chr12:39442677-39442758 | Rare:18 | ||||
| chr12:39442888-39442993 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr12:39443046-39443271 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:39443277-39443482 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:39620035-39620318 | Common:1; Rare:54 | ||||
| chr12:40105961-40106134 | Rare:72 | ||||
| chr12:40224482-40224763 | Common:1; Rare:77 | ||||
| chr12:40224797-40225105 | Common:5; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42144367-42145076 | Common:14; Rare:269 | ||||
| chr12:42237484-42237778 | Rare:94 | ||||
| chr12:42237818-42238076 | Common:2; Rare:52 |