| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:138242180-138242502 | Common:2; Rare:69 | ||||
| chr4:139015280-139015910 | Common:4; Rare:311 | ||||
| chr4:139084192-139084529 | Common:4; Rare:152 | ||||
| chr4:139177132-139177456 | Rare:161 | ||||
| chr4:139295325-139295725 | Common:2; Rare:106 | ||||
| chr4:139301184-139301700 | Common:13; Rare:277 | ||||
| chr4:139302453-139302573 | Common:1; Rare:42 | ||||
| chr4:139453674-139454380 | Common:10; Rare:345; Clinvar:22; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr4:139556181-139556298 | Rare:26 | ||||
| chr4:139665706-139666047 | Common:4; Rare:146 | ||||
| chr4:140373319-140373709 | Common:5; Rare:285 | ||||
| chr4:140427581-140427755 | Common:3; Rare:65 | ||||
| chr4:140756292-140756454 | Rare:63 | ||||
| chr4:141220801-141220989 | Rare:68 | ||||
| chr4:143184628-143184996 | Common:18; Rare:279 |