| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:1973823-1973913 | Rare:38 | ||||
| chr8:2127584-2127818 | Common:7; Rare:46 | ||||
| chr8:6406527-6406680 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708161-6708430 | Common:3; Rare:119 | ||||
| chr8:6708603-6708784 | Common:2; Rare:94 | ||||
| chr8:8386384-8386594 | Common:3; Rare:82 | ||||
| chr8:9150611-9150903 | Common:1; Rare:95 | ||||
| chr8:9151385-9151817 | Common:4; Rare:162 | ||||
| chr8:9555682-9556005 | Common:6; Rare:135 | ||||
| chr8:10839797-10839943 | Rare:63 | ||||
| chr8:11284746-11284848 | Common:2; Rare:46 | ||||
| chr8:11704101-11704210 | Rare:31 | ||||
| chr8:11769569-11769785 | Common:5; Rare:94 | ||||
| chr8:11802440-11802947 | Common:7; Rare:281 | ||||
| chr8:11808314-11808472 | Common:4; Rare:69 |