| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25913998-25914668 | Common:8; Rare:442 | ||||
| chr4:25914730-25915202 | Common:6; Rare:120 | ||||
| chr4:26318890-26319220 | Common:3; Rare:103 | ||||
| chr4:26319230-26319838 | Rare:651 | ||||
| chr4:26319748-26320276 | Common:2; Rare:221 | ||||
| chr4:26320213-26321152 | Common:13; Rare:1386; Clinvar (benign):5 | ||||
| chr4:26583813-26584213 | Common:1; Rare:221 | ||||
| chr4:26584297-26584775 | Common:6; Rare:260 | ||||
| chr4:26857340-26857858 | Common:24; Rare:571 | ||||
| chr4:26860263-26860984 | Common:26; Rare:814 | ||||
| chr4:26861000-26861441 | Common:6; Rare:275 | ||||
| chr4:26861490-26861890 | Common:3; Rare:161 | ||||
| chr4:36244320-36244850 | Common:5; Rare:145 | ||||
| chr4:37686194-37686871 | Common:36; Rare:861 | ||||
| chr4:37826073-37826443 | Common:2; Rare:86 |