| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92393090-92393521 | Common:2; Rare:92 | ||||
| chr9:92482407-92482840 | Rare:57 | ||||
| chr9:92535970-92536216 | Common:1; Rare:32 | ||||
| chr9:92670024-92670341 | Common:1; Rare:94 | ||||
| chr9:92877975-92878076 | Rare:26 | ||||
| chr9:93452297-93452316 | Rare:1 | ||||
| chr9:93453546-93453674 | Rare:26 | ||||
| chr9:94726547-94726695 | Rare:44 | ||||
| chr9:95317663-95317730 | Rare:25; Clinvar:2 | ||||
| chr9:95875449-95875703 | Common:1; Rare:84 | ||||
| chr9:95875985-95876066 | Common:4; Rare:37; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96655293-96655413 | Rare:31 | ||||
| chr9:96778049-96778154 | Rare:33 | ||||
| chr9:97039132-97039308 | Common:1; Rare:64 | ||||
| chr9:97411929-97412162 | Common:2; Rare:64; Clinvar (benign):1 |