| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:30720035-30720422 | Common:2; Rare:84 | ||||
| chr4:37826538-37826729 | Common:6; Rare:68 | ||||
| chr4:38867503-38867830 | Common:2; Rare:96 | ||||
| chr4:39182202-39182548 | Rare:75; Clinvar:2 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527353-39527761 | Common:3; Rare:102 | ||||
| chr4:39527946-39527997 | Rare:10 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 | ||||
| chr4:39697939-39698174 | Common:2; Rare:101 | ||||
| chr4:41990383-41990566 | Common:1; Rare:68 | ||||
| chr4:44678598-44678706 | Rare:50 | ||||
| chr4:44726503-44726635 | Common:1; Rare:49 | ||||
| chr4:48016634-48016784 | Common:1; Rare:44 | ||||
| chr4:48269822-48269981 | Common:1; Rare:30 | ||||
| chr4:48780236-48780572 | Common:2; Rare:101 |