| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38900974-38901339 | Common:2; Rare:86 | ||||
| chr8:38901341-38901442 | Common:1; Rare:30 | ||||
| chr8:38901670-38901851 | Common:3; Rare:31 | ||||
| chr8:38996447-38997073 | Common:7; Rare:237 | ||||
| chr8:40153341-40153841 | Common:2; Rare:162 | ||||
| chr8:41490275-41490631 | Rare:85 | ||||
| chr8:41577985-41578249 | Rare:82 | ||||
| chr8:41664890-41665083 | Common:1; Rare:70 | ||||
| chr8:41665098-41665225 | Rare:29 | ||||
| chr8:41665228-41665299 | Common:1; Rare:17 | ||||
| chr8:41665798-41666108 | Common:1; Rare:58 | ||||
| chr8:41797569-41797803 | Common:2; Rare:64; Clinvar (pathogenic):2 | ||||
| chr8:42338390-42338520 | Common:1; Rare:56 | ||||
| chr8:42391772-42391925 | Common:1; Rare:52 | ||||
| chr8:42540944-42541188 | Common:1; Rare:63 |