| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320514-26320737 | Common:1; Rare:56 | ||||
| chr4:26320871-26321043 | Rare:58; Clinvar (benign):1 | ||||
| chr4:26857409-26857739 | Common:4; Rare:87 | ||||
| chr4:26860563-26860819 | Common:2; Rare:85 | ||||
| chr4:30719904-30720148 | Common:1; Rare:45 | ||||
| chr4:30720771-30720991 | Rare:43 | ||||
| chr4:30721168-30721454 | Common:3; Rare:72 | ||||
| chr4:30721999-30722336 | Common:2; Rare:110 | ||||
| chr4:30722539-30722724 | Common:1; Rare:58 | ||||
| chr4:30724007-30724353 | Common:2; Rare:90 | ||||
| chr4:36244051-36244258 | Common:1; Rare:60 | ||||
| chr4:36244290-36244622 | Common:3; Rare:110 | ||||
| chr4:37826571-37826760 | Common:1; Rare:71 | ||||
| chr4:37890992-37891125 | Common:1; Rare:41 | ||||
| chr4:37977143-37977464 | Rare:83 |