| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541489-42541829 | Common:2; Rare:113 | ||||
| chr8:42541918-42542045 | Rare:35; Clinvar:3 | ||||
| chr8:42542114-42542208 | Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:42843277-42843481 | Common:2; Rare:55; Clinvar (benign):3 | ||||
| chr8:42896298-42896382 | Rare:37 | ||||
| chr8:42896591-42897076 | Common:1; Rare:192 | ||||
| chr8:43056196-43056458 | Rare:105 | ||||
| chr8:47260781-47260981 | Common:3; Rare:87 | ||||
| chr8:47360578-47360805 | Common:1; Rare:29 | ||||
| chr8:47960096-47960203 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960811-47961004 | Common:1; Rare:76; Clinvar:6 | ||||
| chr8:48008348-48008457 | Common:2; Rare:67 | ||||
| chr8:51898955-51899331 | Common:7; Rare:165 | ||||
| chr8:51899523-51899655 | Rare:28 | ||||
| chr8:52714269-52714603 | Common:1; Rare:125 |