| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47659507-47659685 | Common:1; Rare:45 | ||||
| chr8:47960086-47960267 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr8:47960728-47960974 | Common:1; Rare:87; Clinvar:9 | ||||
| chr8:48008220-48008460 | Common:2; Rare:113 | ||||
| chr8:51898955-51899331 | Common:7; Rare:165 | ||||
| chr8:52460918-52461179 | Common:3; Rare:48 | ||||
| chr8:52714174-52714597 | Common:2; Rare:160 | ||||
| chr8:53843189-53843355 | Common:1; Rare:40 | ||||
| chr8:54021908-54022019 | Rare:46 | ||||
| chr8:54022209-54022533 | Common:1; Rare:105 | ||||
| chr8:54135162-54135290 | Common:1; Rare:45 | ||||
| chr8:54457741-54457937 | Common:1; Rare:50 | ||||
| chr8:55773306-55773658 | Common:3; Rare:122 | ||||
| chr8:58553126-58553297 | Rare:61 | ||||
| chr8:58578285-58578458 | Common:4; Rare:23 |