| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121802915-121803114 | Common:1; Rare:51 | ||||
| chr12:122266385-122266525 | Common:1; Rare:65 | ||||
| chr12:122526846-122527282 | Common:4; Rare:157 | ||||
| chr12:122872023-122872205 | Rare:29 | ||||
| chr12:122896048-122896226 | Rare:94 | ||||
| chr12:122980571-122980793 | Common:1; Rare:75 | ||||
| chr12:123233094-123233485 | Common:2; Rare:128; Clinvar:1 | ||||
| chr12:123364812-123364989 | Common:3; Rare:66 | ||||
| chr12:123436622-123436841 | Common:2; Rare:44 | ||||
| chr12:123584314-123584789 | Common:9; Rare:160 | ||||
| chr12:123602031-123602198 | Common:3; Rare:63 | ||||
| chr12:123633607-123633859 | Common:1; Rare:123; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972550-123972656 | Common:3; Rare:33 | ||||
| chr12:124388796-124388962 | Common:3; Rare:47 | ||||
| chr12:124786454-124786786 | Common:3; Rare:88 |