| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:89757661-89757859 | Common:1; Rare:76 | ||||
| chr8:89902410-89902570 | Common:1; Rare:61 | ||||
| chr8:90001377-90001482 | Rare:47 | ||||
| chr8:90985198-90985417 | Common:4; Rare:68 | ||||
| chr8:91069979-91070387 | Common:1; Rare:146 | ||||
| chr8:92966038-92966238 | Common:1; Rare:44 | ||||
| chr8:93700431-93700634 | Common:1; Rare:82 | ||||
| chr8:93740944-93741146 | Rare:72 | ||||
| chr8:93916637-93916969 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr8:94436905-94437069 | Rare:37 | ||||
| chr8:94475010-94475207 | Common:4; Rare:57 | ||||
| chr8:94553431-94553739 | Common:3; Rare:111 | ||||
| chr8:94719738-94719975 | Common:1; Rare:68 | ||||
| chr8:94895704-94895799 | Rare:22 | ||||
| chr8:95133744-95133924 | Common:1; Rare:57 |