| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38231743-38231781 | Rare:8 | ||||
| chr8:38386243-38386507 | Common:1; Rare:54 | ||||
| chr8:38787064-38787249 | Rare:75 | ||||
| chr8:38996461-38996866 | Common:5; Rare:129 | ||||
| chr8:40153446-40153546 | Common:1; Rare:27 | ||||
| chr8:41578390-41578521 | Rare:37 | ||||
| chr8:42338377-42338525 | Common:1; Rare:63 | ||||
| chr8:42391751-42391928 | Common:1; Rare:63 | ||||
| chr8:42541559-42541763 | Rare:74 | ||||
| chr8:42843239-42843508 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896596-42897057 | Common:1; Rare:182 | ||||
| chr8:43056210-43056453 | Rare:98 | ||||
| chr8:43093393-43093539 | Common:1; Rare:29 | ||||
| chr8:47260801-47260991 | Common:3; Rare:81 | ||||
| chr8:47960011-47960230 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):3 |