| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320532-26320826 | Common:1; Rare:95 | ||||
| chr4:26320832-26321045 | Rare:82; Clinvar (benign):1 | ||||
| chr4:26860616-26860812 | Common:2; Rare:65 | ||||
| chr4:30720237-30720432 | Common:1; Rare:50 | ||||
| chr4:36243860-36244082 | Common:2; Rare:48 | ||||
| chr4:37826538-37826728 | Common:6; Rare:67 | ||||
| chr4:37977212-37977447 | Rare:55 | ||||
| chr4:38664194-38664359 | Common:2; Rare:52 | ||||
| chr4:38867564-38867822 | Common:2; Rare:87 | ||||
| chr4:39182202-39182555 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366319-39366397 | Rare:24 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527383-39527775 | Common:2; Rare:103 | ||||
| chr4:39527961-39528079 | Rare:27 | ||||
| chr4:39638634-39639177 | Common:1; Rare:173 |