| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41490359-41490622 | Rare:61 | ||||
| chr8:42338358-42338509 | Common:1; Rare:61 | ||||
| chr8:42540855-42541173 | Rare:78 | ||||
| chr8:42541554-42541661 | Rare:34 | ||||
| chr8:42541674-42542148 | Common:2; Rare:140; Clinvar:4; Clinvar (benign):2 | ||||
| chr8:42843290-42843455 | Common:2; Rare:40; Clinvar (benign):3 | ||||
| chr8:42896573-42896997 | Common:1; Rare:176 | ||||
| chr8:43056115-43056454 | Common:1; Rare:123 | ||||
| chr8:47960693-47961000 | Common:2; Rare:114; Clinvar:9; Clinvar (benign):1 | ||||
| chr8:48008348-48008462 | Common:2; Rare:68 | ||||
| chr8:51899001-51899279 | Common:5; Rare:132 | ||||
| chr8:52714388-52714563 | Common:1; Rare:74 | ||||
| chr8:53880968-53881060 | Common:2; Rare:55 | ||||
| chr8:54022241-54022557 | Common:1; Rare:103 | ||||
| chr8:54101796-54102129 | Common:3; Rare:141 |