| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94615423-94615724 | Common:1; Rare:47 | ||||
| chr12:94615952-94616218 | Rare:51 | ||||
| chr12:94616453-94616526 | Rare:9 | ||||
| chr12:94650454-94650708 | Common:2; Rare:74 | ||||
| chr12:95003596-95003808 | Common:3; Rare:89; Clinvar (benign):6 | ||||
| chr12:95073485-95073672 | Common:1; Rare:69 | ||||
| chr12:95116838-95117088 | Common:1; Rare:58 | ||||
| chr12:95217238-95217877 | Common:6; Rare:183 | ||||
| chr12:95218165-95218321 | Common:2; Rare:37 | ||||
| chr12:95474061-95474328 | Common:2; Rare:114 | ||||
| chr12:95790575-95790878 | Common:2; Rare:83 | ||||
| chr12:95858841-95859073 | Common:1; Rare:65 | ||||
| chr12:95943183-95943343 | Rare:22 | ||||
| chr12:95996285-95996496 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96035352-96035446 | Rare:27 |