| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196082065-196082247 | Common:2; Rare:70 | ||||
| chr3:196318206-196318354 | Common:1; Rare:57 | ||||
| chr3:196639568-196639817 | Common:2; Rare:61 | ||||
| chr3:196712213-196712334 | Common:2; Rare:40 | ||||
| chr3:196867770-196867946 | Rare:63 | ||||
| chr3:196942373-196942702 | Common:1; Rare:143 | ||||
| chr3:197029779-197029938 | Common:1; Rare:51 | ||||
| chr3:197298571-197298763 | Rare:61 | ||||
| chr3:197736841-197737133 | Common:3; Rare:93 | ||||
| chr3:197749782-197750036 | Common:1; Rare:94 | ||||
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197950651-197950978 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959969-197960242 | Common:1; Rare:96 | ||||
| chr4:124290-124520 | Common:6; Rare:58 | ||||
| chr4:337468-337873 | Common:2; Rare:119 |