| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495847-120496201 | Common:7; Rare:122 | ||||
| chr12:120528939-120529179 | Common:2; Rare:94 | ||||
| chr12:120563543-120563942 | Common:1; Rare:109 | ||||
| chr12:120565126-120565527 | Common:1; Rare:109 | ||||
| chr12:120575509-120575865 | Common:3; Rare:93 | ||||
| chr12:120579391-120579571 | Common:2; Rare:57 | ||||
| chr12:120581314-120581548 | Common:1; Rare:92 | ||||
| chr12:120686942-120687234 | Common:2; Rare:100 | ||||
| chr12:120687351-120687525 | Rare:45 | ||||
| chr12:120710625-120710680 | Rare:14 | ||||
| chr12:120903252-120903277 | Common:2; Rare:3 | ||||
| chr12:120978371-120978563 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr12:121209940-121210149 | Common:5; Rare:67 | ||||
| chr12:121352166-121352256 | Rare:34 | ||||
| chr12:121399870-121400163 | Common:5; Rare:107 |