| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41577939-41578256 | Rare:99 | ||||
| chr8:41578374-41578528 | Rare:43 | ||||
| chr8:42051974-42052266 | Common:1; Rare:85 | ||||
| chr8:42152763-42153100 | Common:3; Rare:87 | ||||
| chr8:42271251-42271449 | Common:2; Rare:69 | ||||
| chr8:42338368-42338548 | Common:1; Rare:80 | ||||
| chr8:42391579-42391928 | Common:4; Rare:109 | ||||
| chr8:42540939-42541188 | Common:1; Rare:64 | ||||
| chr8:42541489-42541837 | Common:2; Rare:115 | ||||
| chr8:42541864-42542070 | Rare:50; Clinvar:3 | ||||
| chr8:42842800-42842971 | Common:2; Rare:47 | ||||
| chr8:42843045-42843122 | Rare:23; Clinvar:3 | ||||
| chr8:42843239-42843461 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896289-42896382 | Rare:38 | ||||
| chr8:42896506-42897076 | Common:1; Rare:222 |