| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541451-42541770 | Common:4; Rare:143 | ||||
| chr8:42541691-42541856 | Rare:62 | ||||
| chr8:42542070-42542390 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:42842620-42843110 | Common:7; Rare:233; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr8:42843286-42843514 | Common:4; Rare:118; Clinvar (benign):6 | ||||
| chr8:42896280-42897129 | Common:6; Rare:639 | ||||
| chr8:42897261-42897413 | Common:1; Rare:67 | ||||
| chr8:43056132-43056673 | Common:2; Rare:300 | ||||
| chr8:43093318-43093568 | Common:3; Rare:50; Clinvar (benign):1 | ||||
| chr8:43140250-43140597 | Common:6; Rare:249; Clinvar:19 | ||||
| chr8:47260747-47261012 | Common:6; Rare:213 | ||||
| chr8:47960035-47960280 | Common:4; Rare:174; Clinvar:4; Clinvar (benign):6 | ||||
| chr8:47960668-47961062 | Common:4; Rare:280; Clinvar:21; Clinvar (benign):2 | ||||
| chr8:48008311-48008457 | Common:4; Rare:177 | ||||
| chr8:48008490-48009200 | Rare:263 |