| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110403435-110403795 | Common:3; Rare:138 | ||||
| chr12:110404035-110404194 | Common:4; Rare:36 | ||||
| chr12:110449762-110449967 | Common:1; Rare:39 | ||||
| chr12:110450229-110450559 | Common:2; Rare:106 | ||||
| chr12:110468168-110468599 | Common:3; Rare:140 | ||||
| chr12:110468626-110468937 | Rare:90 | ||||
| chr12:110469209-110469402 | Common:1; Rare:31 | ||||
| chr12:110501963-110502371 | Common:1; Rare:155 | ||||
| chr12:110582669-110582897 | Common:1; Rare:56 | ||||
| chr12:110583201-110583551 | Rare:97 | ||||
| chr12:110613917-110614234 | Rare:94; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110619362-110619581 | Rare:27 | ||||
| chr12:110620289-110620460 | Common:1; Rare:37 | ||||
| chr12:110689060-110689305 | Common:1; Rare:53 | ||||
| chr12:110689397-110689575 | Rare:41 |