| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:104494810-104495039 | Common:1; Rare:51 | ||||
| chr4:104495043-104495100 | Common:1; Rare:9 | ||||
| chr4:105708607-105708865 | Common:2; Rare:85 | ||||
| chr4:105895342-105895515 | Rare:45 | ||||
| chr4:106315923-106316089 | Common:1; Rare:39 | ||||
| chr4:106316146-106316681 | Common:5; Rare:167 | ||||
| chr4:106316779-106316868 | Common:1; Rare:21 | ||||
| chr4:107036301-107036536 | Common:2; Rare:50 | ||||
| chr4:107720151-107720516 | Common:8; Rare:148 | ||||
| chr4:107824641-107824740 | Rare:21 | ||||
| chr4:107989675-107989949 | Common:6; Rare:118; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108167668-108167724 | Rare:12 | ||||
| chr4:108168730-108168817 | Rare:18 | ||||
| chr4:108168836-108168965 | Common:1; Rare:32 | ||||
| chr4:108620378-108620711 | Common:6; Rare:152 |