| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38105441-38105586 | Common:2; Rare:59 | ||||
| chr8:38105775-38105970 | Rare:55 | ||||
| chr8:38176389-38176575 | Common:1; Rare:67 | ||||
| chr8:38176645-38176903 | Common:5; Rare:74 | ||||
| chr8:38231521-38231781 | Rare:71 | ||||
| chr8:38269125-38269262 | Rare:55 | ||||
| chr8:38380627-38380796 | Rare:33 | ||||
| chr8:38381126-38381265 | Rare:28 | ||||
| chr8:38381378-38381755 | Common:1; Rare:55 | ||||
| chr8:38381901-38382031 | Rare:32 | ||||
| chr8:38382069-38382417 | Common:2; Rare:108 | ||||
| chr8:38386390-38386563 | Rare:38 | ||||
| chr8:38467998-38468075 | Rare:23; Clinvar (benign):1 | ||||
| chr8:38996242-38996314 | Common:1; Rare:40 | ||||
| chr8:38996443-38997012 | Common:7; Rare:211 |