| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121672611-121672689 | Common:4; Rare:28 | ||||
| chr12:121712659-121712840 | Common:2; Rare:69 | ||||
| chr12:121802908-121803091 | Rare:48 | ||||
| chr12:121888629-121888863 | Common:2; Rare:75 | ||||
| chr12:122225748-122225827 | Rare:26 | ||||
| chr12:122266405-122266544 | Common:2; Rare:58 | ||||
| chr12:122500846-122501170 | Common:3; Rare:86 | ||||
| chr12:122526864-122527291 | Common:4; Rare:152 | ||||
| chr12:122975151-122975248 | Common:1; Rare:29 | ||||
| chr12:122980571-122980740 | Common:1; Rare:53 | ||||
| chr12:123233096-123233486 | Common:2; Rare:126; Clinvar:1 | ||||
| chr12:123364808-123364989 | Common:3; Rare:68 | ||||
| chr12:123584325-123584816 | Common:8; Rare:163 | ||||
| chr12:123601992-123602164 | Common:3; Rare:60 | ||||
| chr12:123633624-123633860 | Common:1; Rare:110; Clinvar:8; Clinvar (benign):1 |