| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:146521854-146521971 | Rare:23 | ||||
| chr4:146945819-146946007 | Rare:49 | ||||
| chr4:147617242-147617470 | Common:1; Rare:51 | ||||
| chr4:147684088-147684309 | Common:1; Rare:93 | ||||
| chr4:148442346-148442712 | Rare:104; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581819-150582112 | Common:1; Rare:56 | ||||
| chr4:151015707-151015849 | Rare:68 | ||||
| chr4:151099364-151099713 | Common:3; Rare:118 | ||||
| chr4:151100292-151100580 | Common:1; Rare:57 | ||||
| chr4:151408874-151409179 | Common:5; Rare:99 | ||||
| chr4:151760943-151761180 | Rare:97 | ||||
| chr4:152352553-152352684 | Rare:40; Clinvar:1 | ||||
| chr4:152352688-152352971 | Rare:73 | ||||
| chr4:152536056-152536293 | Rare:90 | ||||
| chr4:152779721-152780021 | Common:1; Rare:84 |