| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38996452-38997051 | Common:7; Rare:227 | ||||
| chr8:38997064-38997107 | Rare:18 | ||||
| chr8:41577939-41578274 | Rare:106 | ||||
| chr8:42271251-42271335 | Rare:24 | ||||
| chr8:42338385-42338520 | Common:1; Rare:59 | ||||
| chr8:42391770-42391925 | Common:1; Rare:52 | ||||
| chr8:42540939-42541178 | Rare:62 | ||||
| chr8:42541553-42541759 | Rare:71 | ||||
| chr8:42843045-42843108 | Rare:16; Clinvar:2 | ||||
| chr8:42843290-42843360 | Common:2; Rare:21; Clinvar (benign):3 | ||||
| chr8:42896573-42897056 | Common:1; Rare:189 | ||||
| chr8:43056030-43056454 | Common:2; Rare:141 | ||||
| chr8:43140262-43140602 | Common:3; Rare:130; Clinvar:10 | ||||
| chr8:47260787-47260991 | Common:3; Rare:90 | ||||
| chr8:47959980-47960219 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):4 |