| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98929093-98929203 | Common:3; Rare:34 | ||||
| chr4:98995468-98995748 | Common:6; Rare:102 | ||||
| chr4:99088696-99088891 | Common:6; Rare:90 | ||||
| chr4:99563995-99564107 | Common:2; Rare:35; Clinvar (benign):2 | ||||
| chr4:99894351-99894588 | Common:2; Rare:87 | ||||
| chr4:102826779-102826900 | Rare:32 | ||||
| chr4:102827148-102827425 | Common:1; Rare:96 | ||||
| chr4:102827462-102828129 | Common:4; Rare:223 | ||||
| chr4:102868814-102869082 | Common:2; Rare:92 | ||||
| chr4:105708641-105708827 | Rare:59 | ||||
| chr4:106316173-106316625 | Common:5; Rare:144 | ||||
| chr4:108620384-108620647 | Common:6; Rare:134 | ||||
| chr4:109433757-109433963 | Common:1; Rare:68 | ||||
| chr4:112231565-112231831 | Common:2; Rare:89 | ||||
| chr4:112636886-112637187 | Common:1; Rare:84 |