| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38269132-38269292 | Rare:63 | ||||
| chr8:38996481-38996789 | Common:2; Rare:93 | ||||
| chr8:41490318-41490631 | Rare:73 | ||||
| chr8:41577919-41578262 | Rare:108 | ||||
| chr8:42051970-42052263 | Common:1; Rare:85 | ||||
| chr8:42338377-42338557 | Common:1; Rare:79 | ||||
| chr8:42391784-42391925 | Common:1; Rare:49 | ||||
| chr8:42541044-42541188 | Common:1; Rare:36 | ||||
| chr8:42541494-42541759 | Common:2; Rare:82 | ||||
| chr8:42541902-42541932 | Rare:8 | ||||
| chr8:42843046-42843128 | Rare:26; Clinvar:3 | ||||
| chr8:42843277-42843550 | Common:3; Rare:77; Clinvar (benign):3 | ||||
| chr8:42896676-42896997 | Common:1; Rare:138 | ||||
| chr8:43056120-43056463 | Common:1; Rare:124 | ||||
| chr8:47260787-47260995 | Common:3; Rare:90 |