| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147617204-147617498 | Common:1; Rare:68 | ||||
| chr4:147684080-147684303 | Common:1; Rare:88 | ||||
| chr4:147731844-147732136 | Common:1; Rare:94 | ||||
| chr4:148442310-148442663 | Rare:95; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015191-151015354 | Rare:43 | ||||
| chr4:151015704-151015888 | Rare:81 | ||||
| chr4:151099441-151099728 | Common:3; Rare:105 | ||||
| chr4:151325449-151325827 | Common:4; Rare:106 | ||||
| chr4:151408807-151409218 | Common:5; Rare:129 | ||||
| chr4:151409261-151409460 | Common:3; Rare:36 | ||||
| chr4:151760907-151761146 | Rare:109 | ||||
| chr4:152536047-152536413 | Common:3; Rare:137 | ||||
| chr4:152679986-152680097 | Rare:15 | ||||
| chr4:152779541-152780188 | Common:4; Rare:153 | ||||
| chr4:152935848-152935888 | Rare:11 |