| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98995377-98995755 | Common:6; Rare:134 | ||||
| chr4:99088689-99088884 | Common:6; Rare:93 | ||||
| chr4:99950254-99950476 | Rare:43 | ||||
| chr4:102760916-102761091 | Rare:63; Clinvar:1 | ||||
| chr4:102826643-102826994 | Common:1; Rare:97 | ||||
| chr4:102827465-102827603 | Rare:53 | ||||
| chr4:102827608-102828138 | Common:4; Rare:168 | ||||
| chr4:102868850-102869063 | Common:2; Rare:72 | ||||
| chr4:105708636-105708845 | Common:1; Rare:68 | ||||
| chr4:106316169-106316593 | Common:5; Rare:134 | ||||
| chr4:107824458-107824563 | Rare:19 | ||||
| chr4:107989690-107989907 | Common:5; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620647 | Common:6; Rare:128 | ||||
| chr4:109560090-109560396 | Common:3; Rare:86 | ||||
| chr4:112232139-112232276 | Common:1; Rare:56 |