| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123458417-123458624 | Common:2; Rare:46 | ||||
| chr12:123459771-123459878 | Rare:23 | ||||
| chr12:123533687-123533828 | Common:1; Rare:45 | ||||
| chr12:123584002-123584089 | Rare:11 | ||||
| chr12:123584091-123584651 | Common:6; Rare:158 | ||||
| chr12:123601637-123601698 | Common:1; Rare:5 | ||||
| chr12:123601740-123602225 | Common:6; Rare:127 | ||||
| chr12:123633535-123633917 | Common:2; Rare:178; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123670964-123671216 | Common:5; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:123712060-123712508 | Common:9; Rare:155; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:123761891-123761958 | Rare:16 | ||||
| chr12:123972946-123973346 | Common:2; Rare:125 | ||||
| chr12:124388818-124388983 | Common:3; Rare:48 | ||||
| chr12:124389312-124389445 | Rare:30 | ||||
| chr12:124566950-124567295 | Rare:80 |