| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41577939-41578256 | Rare:99 | ||||
| chr8:42051980-42052034 | Rare:19 | ||||
| chr8:42180240-42180567 | Common:2; Rare:117 | ||||
| chr8:42391529-42391925 | Common:4; Rare:120 | ||||
| chr8:42541041-42541186 | Common:1; Rare:37 | ||||
| chr8:42541556-42541564 | Rare:1 | ||||
| chr8:42541565-42541666 | Rare:34 | ||||
| chr8:42541675-42541750 | Rare:25 | ||||
| chr8:42843045-42843116 | Rare:20; Clinvar:3 | ||||
| chr8:42843277-42843477 | Common:2; Rare:54; Clinvar (benign):3 | ||||
| chr8:42896573-42897027 | Common:1; Rare:183 | ||||
| chr8:43056112-43056499 | Common:1; Rare:139 | ||||
| chr8:47260781-47260981 | Common:3; Rare:87 | ||||
| chr8:47960078-47960230 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:47960805-47961004 | Common:1; Rare:77; Clinvar:6 |