| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827053-102827932 | Common:7; Rare:311 | ||||
| chr4:102827947-102827984 | Rare:10 | ||||
| chr4:102827985-102828151 | Common:1; Rare:61 | ||||
| chr4:102828162-102828299 | Common:2; Rare:41 | ||||
| chr4:102868850-102869087 | Common:2; Rare:84 | ||||
| chr4:103076303-103076372 | Rare:22 | ||||
| chr4:105708628-105708830 | Rare:65 | ||||
| chr4:105895349-105895515 | Rare:44 | ||||
| chr4:106316055-106316613 | Common:5; Rare:174 | ||||
| chr4:106316618-106316621 | |||||
| chr4:107720165-107720516 | Common:7; Rare:141 | ||||
| chr4:107824497-107824746 | Common:1; Rare:53 | ||||
| chr4:107824777-107825055 | Common:1; Rare:85 | ||||
| chr4:107989679-107989974 | Common:6; Rare:128; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108167668-108167752 | Rare:24 |