| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94640713-94641266 | Common:8; Rare:144 | ||||
| chr8:94641290-94641579 | Rare:79 | ||||
| chr8:94664533-94664725 | Common:2; Rare:31 | ||||
| chr8:94719780-94719964 | Common:1; Rare:55 | ||||
| chr8:94895190-94895343 | Rare:51 | ||||
| chr8:94895648-94895822 | Common:1; Rare:51 | ||||
| chr8:94949321-94949548 | Common:2; Rare:69 | ||||
| chr8:95024915-95025199 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133547-95133797 | Common:2; Rare:80 | ||||
| chr8:95133862-95134012 | Common:2; Rare:34 | ||||
| chr8:95268683-95268844 | Common:8; Rare:37 | ||||
| chr8:96261571-96261950 | Common:6; Rare:128 | ||||
| chr8:96645126-96645387 | Common:2; Rare:75 | ||||
| chr8:97277897-97278022 | Rare:41 | ||||
| chr8:97644720-97644884 | Common:1; Rare:52 |