| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:6987034-6987276 | Common:1; Rare:72 | ||||
| chr4:7068037-7068385 | Common:6; Rare:119 | ||||
| chr4:8440717-8440777 | Rare:21 | ||||
| chr4:10116786-10117089 | Common:5; Rare:150 | ||||
| chr4:13484146-13484212 | Common:2; Rare:25 | ||||
| chr4:13484291-13484388 | Rare:44 | ||||
| chr4:15469618-15469896 | Common:1; Rare:56 | ||||
| chr4:15681458-15681901 | Common:4; Rare:154 | ||||
| chr4:17577360-17577545 | Rare:94 | ||||
| chr4:17614537-17614651 | Common:2; Rare:46 | ||||
| chr4:17810701-17811045 | Common:4; Rare:108 | ||||
| chr4:24584435-24584710 | Common:1; Rare:87 | ||||
| chr4:25160388-25160676 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914292 | Common:2; Rare:103 | ||||
| chr4:26320590-26320832 | Common:1; Rare:92 |