| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39458843-39459112 | Common:3; Rare:152; Clinvar (benign):5 | ||||
| chr4:39527327-39527754 | Common:4; Rare:106 | ||||
| chr4:39527961-39527987 | Rare:4 | ||||
| chr4:39638847-39639209 | Common:1; Rare:140 | ||||
| chr4:39697911-39698181 | Common:2; Rare:115 | ||||
| chr4:40056666-40056955 | Common:4; Rare:92 | ||||
| chr4:40335513-40335756 | Common:1; Rare:56 | ||||
| chr4:40629818-40630023 | Common:1; Rare:49 | ||||
| chr4:41216386-41216564 | Common:2; Rare:44 | ||||
| chr4:41990420-41990585 | Common:1; Rare:60 | ||||
| chr4:44678315-44678719 | Common:2; Rare:149 | ||||
| chr4:44726487-44726642 | Common:2; Rare:54 | ||||
| chr4:47463629-47463873 | Common:3; Rare:79 | ||||
| chr4:47485166-47485346 | Common:1; Rare:63 | ||||
| chr4:48016618-48016795 | Common:1; Rare:51 |