| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45990499-45990933 | Common:2; Rare:140 | ||||
| chr12:46268661-46269212 | Common:2; Rare:144 | ||||
| chr12:46372746-46373065 | Common:1; Rare:118 | ||||
| chr12:47705970-47706124 | Rare:67 | ||||
| chr12:47813037-47813343 | Rare:76 | ||||
| chr12:47963417-47963662 | Common:2; Rare:63 | ||||
| chr12:48106031-48106208 | Common:2; Rare:63 | ||||
| chr12:48119186-48119382 | Common:2; Rare:38; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48119601-48119824 | Rare:46 | ||||
| chr12:48716671-48717008 | Common:4; Rare:101 | ||||
| chr12:48852127-48852338 | Common:2; Rare:63 | ||||
| chr12:48925490-48925612 | Rare:21 | ||||
| chr12:48957434-48957581 | Common:1; Rare:43 | ||||
| chr12:49018739-49018935 | Common:1; Rare:81 | ||||
| chr12:49069934-49070144 | Common:2; Rare:54 |