| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94757678-94758053 | Common:4; Rare:115 | ||||
| chr4:95548814-95548980 | Common:1; Rare:69 | ||||
| chr4:95548985-95549294 | Common:2; Rare:67 | ||||
| chr4:98143416-98143639 | Common:1; Rare:57 | ||||
| chr4:98261153-98261510 | Common:1; Rare:113 | ||||
| chr4:98657618-98657811 | Rare:36 | ||||
| chr4:98658605-98658760 | Common:1; Rare:48 | ||||
| chr4:98928978-98929349 | Common:3; Rare:110 | ||||
| chr4:98995403-98995765 | Common:6; Rare:129 | ||||
| chr4:99088696-99088891 | Common:6; Rare:90 | ||||
| chr4:99563564-99563825 | Common:2; Rare:78 | ||||
| chr4:99563969-99564170 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894330-99894620 | Common:3; Rare:99 | ||||
| chr4:99946506-99946880 | Rare:131 | ||||
| chr4:99949685-99949991 | Common:3; Rare:102 |