| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99088708-99088891 | Common:6; Rare:80 | ||||
| chr4:99563989-99564123 | Common:2; Rare:43; Clinvar (benign):2 | ||||
| chr4:99894357-99894635 | Common:3; Rare:92 | ||||
| chr4:99949723-99949964 | Common:3; Rare:88 | ||||
| chr4:99950259-99950527 | Rare:54 | ||||
| chr4:101347602-101347835 | Common:4; Rare:67 | ||||
| chr4:102760916-102761040 | Rare:41; Clinvar:1 | ||||
| chr4:102826754-102826969 | Rare:62 | ||||
| chr4:102827081-102827261 | Rare:64 | ||||
| chr4:102827456-102827969 | Common:4; Rare:173 | ||||
| chr4:102827997-102828151 | Common:1; Rare:58 | ||||
| chr4:102868850-102869087 | Common:2; Rare:84 | ||||
| chr4:103076295-103076398 | Rare:31 | ||||
| chr4:104494827-104495219 | Common:3; Rare:87 | ||||
| chr4:105552319-105552722 | Rare:62 |