| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6383988-6384225 | Common:1; Rare:54 | ||||
| chr12:6493088-6493386 | Common:7; Rare:88 | ||||
| chr12:6493746-6494001 | Common:2; Rare:85 | ||||
| chr12:6534232-6534578 | Common:6; Rare:134 | ||||
| chr12:6536491-6536817 | Rare:106 | ||||
| chr12:6568234-6568357 | Rare:45 | ||||
| chr12:6688887-6689188 | Rare:93 | ||||
| chr12:6689386-6689750 | Common:3; Rare:99 | ||||
| chr12:6723792-6724172 | Common:1; Rare:82 | ||||
| chr12:6851912-6852181 | Rare:69 | ||||
| chr12:6867387-6867665 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873330-6873532 | Common:1; Rare:57 | ||||
| chr12:6943789-6944172 | Common:16; Rare:400; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6967602-6967774 | Rare:44 | ||||
| chr12:6970612-6970952 | Common:3; Rare:105 |