| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:101347570-101347823 | Common:4; Rare:78 | ||||
| chr4:102760911-102761052 | Rare:47; Clinvar:1 | ||||
| chr4:102827148-102827436 | Common:1; Rare:100 | ||||
| chr4:102827439-102827969 | Common:4; Rare:176 | ||||
| chr4:102827985-102828151 | Common:1; Rare:61 | ||||
| chr4:102868850-102869082 | Common:2; Rare:83 | ||||
| chr4:103019660-103019791 | Common:1; Rare:40 | ||||
| chr4:105708641-105708865 | Common:2; Rare:74 | ||||
| chr4:106316135-106316601 | Common:5; Rare:151 | ||||
| chr4:106316609-106316635 | Rare:11 | ||||
| chr4:107720166-107720447 | Common:7; Rare:113 | ||||
| chr4:107824409-107824693 | Common:1; Rare:59 | ||||
| chr4:107989679-107989907 | Common:6; Rare:107; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620384-108620668 | Common:6; Rare:140 | ||||
| chr4:109433756-109433947 | Common:1; Rare:63 |