| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77187190-77187590 | Common:1; Rare:91 | ||||
| chr4:77862596-77862947 | Common:3; Rare:128 | ||||
| chr4:78057451-78057613 | Common:2; Rare:36 | ||||
| chr4:78776199-78776477 | Common:1; Rare:116 | ||||
| chr4:78939352-78939519 | Common:2; Rare:79 | ||||
| chr4:79964560-79965410 | Common:7; Rare:198 | ||||
| chr4:80072144-80072439 | Common:2; Rare:73 | ||||
| chr4:80073058-80073206 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:80184056-80184591 | Common:6; Rare:161 | ||||
| chr4:80185422-80186034 | Common:5; Rare:170 | ||||
| chr4:80197175-80197508 | Common:3; Rare:69 | ||||
| chr4:81471902-81472107 | Rare:78 | ||||
| chr4:82044281-82044534 | Common:2; Rare:71 | ||||
| chr4:82372948-82373739 | Common:2; Rare:480 | ||||
| chr4:82373948-82374364 | Common:4; Rare:130 |