| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:663595-663727 | Rare:43 | ||||
| chr4:673842-673952 | Rare:47 | ||||
| chr4:674243-674599 | Common:3; Rare:168 | ||||
| chr4:680934-681227 | Rare:109 | ||||
| chr4:689141-689411 | Common:3; Rare:70 | ||||
| chr4:932216-932487 | Common:2; Rare:106 | ||||
| chr4:986930-987158 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113524-1113627 | Common:2; Rare:37 | ||||
| chr4:1172802-1173078 | Common:5; Rare:41 | ||||
| chr4:1249963-1250147 | Common:4; Rare:37 | ||||
| chr4:1289656-1289924 | Common:1; Rare:90 | ||||
| chr4:1346816-1347083 | Common:4; Rare:79 | ||||
| chr4:1720538-1720638 | Rare:29 | ||||
| chr4:1723253-1723551 | Common:4; Rare:85 | ||||
| chr4:2468878-2469187 | Common:4; Rare:122 |