| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41490227-41490648 | Rare:101 | ||||
| chr8:41577956-41578274 | Rare:102 | ||||
| chr8:42051954-42052263 | Common:1; Rare:87 | ||||
| chr8:42152702-42153105 | Common:3; Rare:108 | ||||
| chr8:42207516-42207860 | Common:2; Rare:83 | ||||
| chr8:42271251-42271337 | Rare:26 | ||||
| chr8:42338399-42338525 | Common:1; Rare:55 | ||||
| chr8:42391766-42391925 | Common:1; Rare:53 | ||||
| chr8:42541113-42541194 | Common:1; Rare:19 | ||||
| chr8:42541494-42542070 | Common:3; Rare:175; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42842793-42843013 | Common:2; Rare:70 | ||||
| chr8:42843045-42843092 | Rare:11; Clinvar:2 | ||||
| chr8:42843277-42843489 | Common:2; Rare:58; Clinvar (benign):3 | ||||
| chr8:42896283-42896383 | Rare:42 | ||||
| chr8:42896552-42897027 | Common:1; Rare:191 |