| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38176430-38176890 | Common:6; Rare:133 | ||||
| chr8:38996451-38996821 | Common:4; Rare:124 | ||||
| chr8:41490348-41490622 | Rare:63 | ||||
| chr8:42391778-42391925 | Common:1; Rare:50 | ||||
| chr8:42541555-42541661 | Rare:34 | ||||
| chr8:42541691-42541882 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr8:42843290-42843477 | Common:2; Rare:51; Clinvar (benign):3 | ||||
| chr8:43056198-43056463 | Rare:104 | ||||
| chr8:47260790-47260981 | Common:3; Rare:82 | ||||
| chr8:47960122-47960267 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr8:47960668-47961000 | Common:2; Rare:129; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:51898972-51899326 | Common:7; Rare:156 | ||||
| chr8:53843218-53843346 | Rare:28 | ||||
| chr8:54022143-54022452 | Common:1; Rare:97 | ||||
| chr8:54101780-54102140 | Common:3; Rare:147 |