| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38426163-38426393 | Rare:45; Clinvar:1 | ||||
| chr8:38466191-38466292 | Common:1; Rare:34 | ||||
| chr8:38467985-38468164 | Rare:51; Clinvar (benign):2 | ||||
| chr8:38727980-38728213 | Common:2; Rare:47 | ||||
| chr8:38728241-38728681 | Common:4; Rare:84 | ||||
| chr8:38786988-38787234 | Rare:91 | ||||
| chr8:38901055-38901378 | Common:2; Rare:77 | ||||
| chr8:38996443-38997107 | Common:7; Rare:254 | ||||
| chr8:38997235-38997553 | Common:1; Rare:72 | ||||
| chr8:40153319-40153502 | Common:1; Rare:39 | ||||
| chr8:41490248-41490631 | Rare:89 | ||||
| chr8:41577939-41578274 | Rare:106 | ||||
| chr8:42051960-42052266 | Common:1; Rare:86 | ||||
| chr8:42152733-42153089 | Common:3; Rare:91 | ||||
| chr8:42271241-42271449 | Common:2; Rare:73 |