| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:80197250-80197508 | Common:3; Rare:56 | ||||
| chr4:80266413-80267111 | Common:4; Rare:233; Clinvar (pathogenic):1 | ||||
| chr4:82373428-82374055 | Rare:226 | ||||
| chr4:82374122-82374191 | Rare:21 | ||||
| chr4:82429247-82429653 | Common:2; Rare:218; Clinvar:13; Clinvar (benign):8 | ||||
| chr4:82429878-82430308 | Common:2; Rare:125 | ||||
| chr4:82430402-82430871 | Common:3; Rare:167 | ||||
| chr4:82866902-82867231 | Common:1; Rare:87 | ||||
| chr4:82891001-82891331 | Common:2; Rare:124 | ||||
| chr4:82900334-82900741 | Common:1; Rare:107 | ||||
| chr4:82900927-82901217 | Common:2; Rare:99 | ||||
| chr4:83012916-83013231 | Common:1; Rare:89 | ||||
| chr4:83034849-83035252 | Common:1; Rare:103 | ||||
| chr4:83114698-83114937 | Common:3; Rare:38 | ||||
| chr4:83284559-83284899 | Common:3; Rare:141; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):2 |