| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:20254137-20254298 | Common:1; Rare:33 | ||||
| chr4:24584356-24584725 | Common:1; Rare:113 | ||||
| chr4:24795308-24795646 | Common:1; Rare:75 | ||||
| chr4:24912856-24913129 | Common:1; Rare:95 | ||||
| chr4:25160388-25160740 | Common:3; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233847-25234050 | Rare:88 | ||||
| chr4:25914051-25914316 | Common:2; Rare:114 | ||||
| chr4:26320893-26321043 | Rare:53; Clinvar (benign):1 | ||||
| chr4:26860624-26860807 | Common:1; Rare:60 | ||||
| chr4:30721168-30721443 | Common:3; Rare:69 | ||||
| chr4:30721970-30722182 | Common:1; Rare:65 | ||||
| chr4:30724180-30724347 | Rare:45 | ||||
| chr4:37826544-37826752 | Common:6; Rare:78 | ||||
| chr4:37890515-37890619 | Common:1; Rare:20 | ||||
| chr4:37890712-37890844 | Rare:30 |