| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:104494816-104495191 | Common:3; Rare:79 | ||||
| chr4:105146561-105146919 | Common:2; Rare:115 | ||||
| chr4:105473222-105473529 | Rare:85 | ||||
| chr4:105708636-105708882 | Common:3; Rare:79 | ||||
| chr4:105895361-105895527 | Rare:45 | ||||
| chr4:106316173-106316694 | Common:5; Rare:158 | ||||
| chr4:107720165-107720556 | Common:7; Rare:161 | ||||
| chr4:107989679-107989949 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108168721-108168798 | Rare:15 | ||||
| chr4:108168818-108168904 | Common:1; Rare:20 | ||||
| chr4:108168915-108169107 | Common:1; Rare:42 | ||||
| chr4:108620355-108620718 | Common:6; Rare:164 | ||||
| chr4:109302742-109303069 | Common:6; Rare:88 | ||||
| chr4:109433482-109433627 | Common:1; Rare:41 | ||||
| chr4:109433750-109433948 | Common:1; Rare:64 |