| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541555-42541671 | Rare:39 | ||||
| chr8:42541685-42541930 | Common:1; Rare:79; Clinvar (benign):1 | ||||
| chr8:42843047-42843095 | Rare:10; Clinvar:2 | ||||
| chr8:42896591-42897048 | Common:1; Rare:183 | ||||
| chr8:43056196-43056454 | Rare:105 | ||||
| chr8:47960106-47960267 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960716-47960974 | Common:1; Rare:94; Clinvar:9 | ||||
| chr8:48008322-48008456 | Common:2; Rare:84 | ||||
| chr8:51898972-51899255 | Common:6; Rare:131 | ||||
| chr8:53843212-53843314 | Rare:24 | ||||
| chr8:54022261-54022510 | Common:1; Rare:79 | ||||
| chr8:55773302-55773497 | Common:3; Rare:61 | ||||
| chr8:56074413-56074741 | Common:6; Rare:131 | ||||
| chr8:59119106-59119270 | Rare:45 | ||||
| chr8:60516838-60517222 | Common:1; Rare:121 |