| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196942373-196942680 | Common:1; Rare:129 | ||||
| chr3:197029780-197029932 | Common:1; Rare:49 | ||||
| chr3:197555950-197556049 | Rare:24 | ||||
| chr3:197736820-197737147 | Common:3; Rare:105 | ||||
| chr3:197749777-197750002 | Common:1; Rare:84 | ||||
| chr3:197949894-197950250 | Common:4; Rare:110; Clinvar (benign):2 | ||||
| chr3:197950795-197950978 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959934-197960242 | Common:1; Rare:105 | ||||
| chr4:337544-337918 | Common:5; Rare:100 | ||||
| chr4:474105-474481 | Common:3; Rare:123 | ||||
| chr4:499141-499319 | Common:2; Rare:65 | ||||
| chr4:674212-674627 | Common:4; Rare:188 | ||||
| chr4:681120-681235 | Rare:46 | ||||
| chr4:705588-705927 | Common:1; Rare:113 | ||||
| chr4:932250-932487 | Common:2; Rare:93 |