| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38382134-38382417 | Common:2; Rare:90 | ||||
| chr8:38386332-38386538 | Common:1; Rare:45 | ||||
| chr8:38467997-38468096 | Rare:29; Clinvar (benign):1 | ||||
| chr8:38996475-38997038 | Common:5; Rare:204 | ||||
| chr8:40153319-40153482 | Rare:32 | ||||
| chr8:41490359-41490651 | Common:1; Rare:72 | ||||
| chr8:41577939-41578266 | Rare:103 | ||||
| chr8:42051954-42052266 | Common:1; Rare:87 | ||||
| chr8:42391592-42391927 | Common:4; Rare:107 | ||||
| chr8:42541040-42541189 | Common:1; Rare:38 | ||||
| chr8:42541484-42541910 | Common:3; Rare:131; Clinvar (benign):1 | ||||
| chr8:42542000-42542154 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):2 | ||||
| chr8:42842786-42842996 | Common:2; Rare:66 | ||||
| chr8:42843045-42843087 | Rare:11; Clinvar:2 | ||||
| chr8:42843277-42843511 | Common:2; Rare:67; Clinvar (benign):3 |