| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541494-42541666 | Common:2; Rare:47 | ||||
| chr8:42541668-42541741 | Rare:26 | ||||
| chr8:42541917-42542230 | Common:1; Rare:81; Clinvar:4; Clinvar (benign):2 | ||||
| chr8:42843290-42843431 | Common:2; Rare:35; Clinvar (benign):3 | ||||
| chr8:42896573-42896996 | Common:1; Rare:176 | ||||
| chr8:43056105-43056477 | Common:1; Rare:132 | ||||
| chr8:43140284-43140583 | Common:3; Rare:115; Clinvar:9 | ||||
| chr8:47260781-47260981 | Common:3; Rare:87 | ||||
| chr8:47960084-47960267 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr8:47960796-47961000 | Common:1; Rare:78; Clinvar:7 | ||||
| chr8:51898955-51899347 | Common:8; Rare:173 | ||||
| chr8:51899616-51899649 | Rare:6 | ||||
| chr8:52714427-52714616 | Common:1; Rare:82 | ||||
| chr8:53843212-53843358 | Rare:35 | ||||
| chr8:54022247-54022510 | Common:1; Rare:84 |