| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25914034-25914308 | Common:2; Rare:119 | ||||
| chr4:26320765-26321028 | Rare:108; Clinvar (benign):1 | ||||
| chr4:37826538-37826723 | Common:6; Rare:66 | ||||
| chr4:38867606-38867822 | Common:2; Rare:81 | ||||
| chr4:39458857-39459065 | Common:3; Rare:116 | ||||
| chr4:39527426-39527755 | Common:2; Rare:83 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 | ||||
| chr4:39697897-39698185 | Common:2; Rare:121 | ||||
| chr4:40056703-40056935 | Common:4; Rare:81 | ||||
| chr4:47485166-47485340 | Common:1; Rare:62 | ||||
| chr4:48341266-48341494 | Rare:91 | ||||
| chr4:51842810-51843212 | Common:1; Rare:119 | ||||
| chr4:52659204-52659439 | Common:1; Rare:80 | ||||
| chr4:53366003-53366164 | Rare:35 | ||||
| chr4:55546815-55547012 | Common:2; Rare:68 |