| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76763905-76764276 | Common:5; Rare:151 | ||||
| chr12:76878942-76879207 | Rare:92 | ||||
| chr12:79690446-79690657 | Rare:59 | ||||
| chr12:79690756-79690794 | Rare:10 | ||||
| chr12:79690927-79691218 | Common:1; Rare:94 | ||||
| chr12:79934795-79935269 | Common:1; Rare:170 | ||||
| chr12:79935271-79935396 | Rare:44 | ||||
| chr12:80444275-80444514 | Common:1; Rare:57; Clinvar (benign):2 | ||||
| chr12:80707222-80707485 | Common:2; Rare:48 | ||||
| chr12:80937659-80937859 | Common:1; Rare:61 | ||||
| chr12:81078009-81078203 | Rare:58 | ||||
| chr12:82358299-82358568 | Common:1; Rare:127 | ||||
| chr12:82358727-82358896 | Common:3; Rare:89 | ||||
| chr12:82686415-82686585 | Rare:32 | ||||
| chr12:82686732-82687164 | Common:3; Rare:136 |