| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:73998564-73998816 | Rare:64 | ||||
| chr4:74038685-74038908 | Rare:63 | ||||
| chr4:74157901-74158188 | Common:1; Rare:133 | ||||
| chr4:75514253-75514507 | Common:1; Rare:91 | ||||
| chr4:75514652-75514763 | Rare:29 | ||||
| chr4:75630441-75630650 | Rare:48 | ||||
| chr4:75673074-75673222 | Rare:36 | ||||
| chr4:75673250-75673648 | Common:1; Rare:153 | ||||
| chr4:75724375-75724810 | Common:2; Rare:131 | ||||
| chr4:76148346-76148561 | Common:3; Rare:71 | ||||
| chr4:76213518-76213988 | Common:4; Rare:165; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:76251528-76251739 | Common:1; Rare:48 | ||||
| chr4:76585926-76586315 | Common:3; Rare:81 | ||||
| chr4:76897967-76898317 | Common:1; Rare:76 | ||||
| chr4:76949559-76949905 | Common:2; Rare:116 |