| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:78776225-78776408 | Common:1; Rare:148 | ||||
| chr4:78939337-78939565 | Common:4; Rare:203 | ||||
| chr4:82373769-82374191 | Common:4; Rare:217 | ||||
| chr4:82374220-82374730 | Common:5; Rare:269 | ||||
| chr4:82429371-82429653 | Common:2; Rare:330; Clinvar:24; Clinvar (benign):12 | ||||
| chr4:82429958-82430103 | Rare:40 | ||||
| chr4:82430166-82430671 | Common:4; Rare:317 | ||||
| chr4:82891008-82891449 | Common:4; Rare:281 | ||||
| chr4:82900454-82900858 | Rare:209 | ||||
| chr4:82900870-82901190 | Common:3; Rare:244 | ||||
| chr4:83010717-83011140 | Rare:85 | ||||
| chr4:83012823-83013300 | Common:3; Rare:231 | ||||
| chr4:83034841-83035236 | Common:2; Rare:195 | ||||
| chr4:83114698-83114810 | Common:2; Rare:25 | ||||
| chr4:83284420-83284690 | Common:2; Rare:182; Clinvar:12; Clinvar (benign):5; Clinvar (pathogenic):4 |