| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139028290-139028569 | Common:2; Rare:57 | ||||
| chr4:139177892-139178171 | Rare:87 | ||||
| chr4:139387725-139388040 | Common:1; Rare:62 | ||||
| chr4:140426757-140426915 | Rare:45 | ||||
| chr4:141332584-141332936 | Common:1; Rare:94 | ||||
| chr4:143350212-143350468 | Common:2; Rare:49 | ||||
| chr4:147822281-147822448 | Rare:22 | ||||
| chr4:151799232-151799430 | Common:3; Rare:33 | ||||
| chr4:152691332-152691538 | Common:1; Rare:33 | ||||
| chr4:158670904-158671172 | Common:3; Rare:38 | ||||
| chr4:158841521-158841813 | Common:1; Rare:38 | ||||
| chr4:168498337-168498552 | Common:3; Rare:38 | ||||
| chr4:168924025-168924429 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:173507828-173508131 | Common:1; Rare:74 | ||||
| chr4:173508377-173508524 | Common:2; Rare:21 |