| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15655280-15655593 | Common:1; Rare:143 | ||||
| chr4:15659818-15660142 | Common:1; Rare:62 | ||||
| chr4:15681542-15681863 | Common:3; Rare:115 | ||||
| chr4:15703008-15703137 | Common:1; Rare:28 | ||||
| chr4:17614553-17614655 | Common:2; Rare:42 | ||||
| chr4:24584463-24584727 | Common:1; Rare:80 | ||||
| chr4:25160405-25160732 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233854-25234061 | Rare:90 | ||||
| chr4:26320523-26320866 | Common:1; Rare:126 | ||||
| chr4:26320874-26321045 | Rare:59; Clinvar (benign):1 | ||||
| chr4:26430229-26430937 | Common:2; Rare:155 | ||||
| chr4:26860534-26860825 | Common:4; Rare:95 | ||||
| chr4:37826603-37826741 | Common:1; Rare:55 | ||||
| chr4:39366330-39366460 | Rare:42 | ||||
| chr4:39455381-39455535 | Common:1; Rare:29 |