| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:76007108-76007508 | Common:5; Rare:173 | ||||
| chr4:76147520-76148080 | Common:6; Rare:175 | ||||
| chr4:76148267-76148631 | Common:14; Rare:255 | ||||
| chr4:76212965-76213546 | Common:9; Rare:201; Clinvar:2; Clinvar (benign):6 | ||||
| chr4:76213491-76214119 | Common:12; Rare:521; Clinvar:3; Clinvar (benign):14 | ||||
| chr4:76235969-76236099 | Common:2; Rare:24 | ||||
| chr4:76236040-76236410 | Common:8; Rare:88 | ||||
| chr4:76251513-76251780 | Common:1; Rare:99 | ||||
| chr4:76305808-76306120 | Common:2; Rare:87 | ||||
| chr4:76306057-76306461 | Common:8; Rare:147 | ||||
| chr4:76306455-76306819 | Common:3; Rare:264 | ||||
| chr4:76420910-76421730 | Common:20; Rare:251 | ||||
| chr4:76585950-76586458 | Common:8; Rare:193 | ||||
| chr4:76689143-76689667 | Common:5; Rare:219 | ||||
| chr4:76689934-76690570 | Common:4; Rare:121 |