| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21751146-21751964 | Common:5; Rare:235 | ||||
| chr12:21888402-21888840 | Rare:138 | ||||
| chr12:22304432-22304894 | Common:3; Rare:84 | ||||
| chr12:23235300-23235710 | Common:3; Rare:113 | ||||
| chr12:23472270-23472750 | Common:6; Rare:154 | ||||
| chr12:24069790-24070360 | Common:1; Rare:107 | ||||
| chr12:24463379-24463671 | Common:3; Rare:57 | ||||
| chr12:24544780-24545210 | Common:1; Rare:90 | ||||
| chr12:24560207-24560453 | Rare:44 | ||||
| chr12:24562845-24563154 | Rare:74 | ||||
| chr12:25226778-25227435 | Common:7; Rare:236; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr12:25249815-25250282 | Common:5; Rare:153 | ||||
| chr12:25386114-25386468 | Common:6; Rare:299 | ||||
| chr12:25386470-25386810 | Common:3; Rare:71 | ||||
| chr12:25488950-25489320 | Common:5; Rare:115 |