| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:24912849-24913176 | Common:3; Rare:109 | ||||
| chr4:25160343-25160728 | Common:3; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234074 | Rare:98 | ||||
| chr4:25376955-25377338 | Common:4; Rare:113 | ||||
| chr4:26320450-26320832 | Common:1; Rare:120 | ||||
| chr4:26320873-26321045 | Rare:59; Clinvar (benign):1 | ||||
| chr4:26583971-26584124 | Rare:31 | ||||
| chr4:26860548-26860798 | Common:2; Rare:76 | ||||
| chr4:37826538-37826760 | Common:6; Rare:82 | ||||
| chr4:37977173-37977459 | Rare:68 | ||||
| chr4:38664194-38664291 | Common:1; Rare:33 | ||||
| chr4:38867617-38867846 | Common:2; Rare:83 | ||||
| chr4:38868066-38868114 | Rare:15 | ||||
| chr4:39044739-39045062 | Common:6; Rare:90 | ||||
| chr4:39182202-39182554 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 |