| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541680-42542045 | Common:1; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42843027-42843099 | Rare:18; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr8:42843277-42843511 | Common:2; Rare:67; Clinvar (benign):3 | ||||
| chr8:42896627-42897027 | Common:1; Rare:161 | ||||
| chr8:43056132-43056454 | Common:1; Rare:119 | ||||
| chr8:47260781-47260991 | Common:3; Rare:93 | ||||
| chr8:47960112-47960267 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr8:47960683-47961000 | Common:2; Rare:121; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:48008220-48008467 | Common:2; Rare:116 | ||||
| chr8:51898955-51899347 | Common:8; Rare:173 | ||||
| chr8:51899526-51899655 | Rare:28 | ||||
| chr8:52714421-52714613 | Common:1; Rare:85 | ||||
| chr8:53843234-53843328 | Rare:19 | ||||
| chr8:54022241-54022514 | Common:1; Rare:89 | ||||
| chr8:54135153-54135301 | Common:2; Rare:47 |