| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:148442323-148442749 | Rare:125; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015718-151015817 | Rare:40 | ||||
| chr4:151099491-151099667 | Common:3; Rare:74 | ||||
| chr4:151408871-151409267 | Common:5; Rare:125 | ||||
| chr4:151409349-151409446 | Rare:19 | ||||
| chr4:152536054-152536293 | Rare:91 | ||||
| chr4:152779715-152780015 | Common:1; Rare:84 | ||||
| chr4:152936129-152936393 | Common:4; Rare:69 | ||||
| chr4:156971797-156972026 | Common:2; Rare:83 | ||||
| chr4:158173012-158173090 | Rare:15 | ||||
| chr4:158671856-158672162 | Common:4; Rare:77; Clinvar:1 | ||||
| chr4:158672199-158672359 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:163166826-163166973 | Common:2; Rare:48 | ||||
| chr4:164956932-164957033 | Common:2; Rare:33 | ||||
| chr4:165327411-165327741 | Common:2; Rare:95 |