| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:18084787-18084852 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr8:18084922-18085027 | Rare:25 | ||||
| chr8:21919486-21919772 | Common:2; Rare:116 | ||||
| chr8:22245024-22245192 | Common:1; Rare:83 | ||||
| chr8:22367053-22367331 | Common:6; Rare:93 | ||||
| chr8:22440980-22441344 | Common:6; Rare:97 | ||||
| chr8:22604520-22604829 | Common:1; Rare:115 | ||||
| chr8:22927710-22928005 | Common:4; Rare:69 | ||||
| chr8:23225082-23225205 | Common:1; Rare:30 | ||||
| chr8:23457605-23457778 | Common:3; Rare:67 | ||||
| chr8:26045359-26045562 | Common:2; Rare:76 | ||||
| chr8:26382930-26383166 | Common:3; Rare:109 | ||||
| chr8:26513870-26514034 | Common:1; Rare:29 | ||||
| chr8:26866976-26867290 | Common:1; Rare:68 | ||||
| chr8:27311236-27311478 | Common:7; Rare:95 |