| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:88389012-88389179 | Common:1; Rare:61 | ||||
| chr9:88389188-88389320 | Rare:50 | ||||
| chr9:89310882-89311239 | Common:4; Rare:126 | ||||
| chr9:89318409-89318612 | Common:5; Rare:94 | ||||
| chr9:89604807-89605033 | Common:6; Rare:57 | ||||
| chr9:90801663-90801938 | Common:2; Rare:82 | ||||
| chr9:91361760-91362006 | Common:2; Rare:91; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr9:91950208-91950423 | Common:2; Rare:60 | ||||
| chr9:92108739-92108932 | Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:92115330-92115509 | Common:1; Rare:57; Clinvar:1 | ||||
| chr9:92293581-92293890 | Common:5; Rare:100 | ||||
| chr9:92310594-92310827 | Common:1; Rare:59 | ||||
| chr9:92325299-92326033 | Common:9; Rare:201 | ||||
| chr9:92404547-92404704 | Rare:35 | ||||
| chr9:92535978-92536035 | Rare:9 |