| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74157901-74158184 | Common:1; Rare:131 | ||||
| chr4:74365254-74365322 | Rare:37 | ||||
| chr4:74365362-74365437 | Rare:22 | ||||
| chr4:74444923-74445148 | Common:1; Rare:45 | ||||
| chr4:75514273-75514507 | Common:1; Rare:81 | ||||
| chr4:75514664-75514737 | Rare:20 | ||||
| chr4:75630484-75630632 | Rare:35 | ||||
| chr4:75673290-75673648 | Common:1; Rare:141 | ||||
| chr4:75724365-75724829 | Common:2; Rare:138 | ||||
| chr4:76148357-76148577 | Common:3; Rare:70 | ||||
| chr4:76213425-76214005 | Common:5; Rare:195; Clinvar:3; Clinvar (benign):9 | ||||
| chr4:76251568-76251744 | Rare:41 | ||||
| chr4:76949559-76949906 | Common:2; Rare:116 | ||||
| chr4:77028356-77028655 | Common:3; Rare:58 | ||||
| chr4:77075944-77076126 | Common:3; Rare:99 |