| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196941875-196941972 | Rare:34 | ||||
| chr3:196942375-196942689 | Common:1; Rare:133 | ||||
| chr3:197736882-197737154 | Common:3; Rare:86 | ||||
| chr3:197749795-197749962 | Common:1; Rare:66 | ||||
| chr3:197949894-197950306 | Common:4; Rare:124; Clinvar (benign):2 | ||||
| chr3:197950961-197951248 | Rare:84; Clinvar (benign):1 | ||||
| chr3:197959982-197960248 | Common:1; Rare:93 | ||||
| chr4:499141-499318 | Common:2; Rare:65 | ||||
| chr4:673820-673982 | Common:1; Rare:64 | ||||
| chr4:674212-674599 | Common:4; Rare:180 | ||||
| chr4:705578-705953 | Common:1; Rare:127 | ||||
| chr4:932264-932497 | Common:2; Rare:90 | ||||
| chr4:986936-987029 | Rare:23; Clinvar:1 | ||||
| chr4:1289659-1289924 | Common:1; Rare:88 | ||||
| chr4:1309404-1309668 | Common:3; Rare:72 |