| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42051962-42052254 | Common:1; Rare:82 | ||||
| chr8:42207533-42207869 | Common:2; Rare:80 | ||||
| chr8:42271251-42271335 | Rare:24 | ||||
| chr8:42391529-42391919 | Common:4; Rare:118 | ||||
| chr8:42541101-42541182 | Rare:18 | ||||
| chr8:42541554-42541765 | Rare:75 | ||||
| chr8:42542137-42542278 | Rare:40; Clinvar (benign):1 | ||||
| chr8:42843256-42843469 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896596-42897081 | Common:1; Rare:192 | ||||
| chr8:43056210-43056362 | Rare:56 | ||||
| chr8:43140302-43140583 | Common:3; Rare:108; Clinvar:9 | ||||
| chr8:47260796-47260991 | Common:3; Rare:85 | ||||
| chr8:47960123-47960267 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr8:47960811-47961006 | Common:1; Rare:77; Clinvar:6 | ||||
| chr8:51898957-51899334 | Common:8; Rare:166 |