| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33402415-33402747 | Rare:69 | ||||
| chr9:33473847-33474144 | Common:4; Rare:92 | ||||
| chr9:34049175-34049263 | Common:1; Rare:22 | ||||
| chr9:34126631-34126786 | Rare:51 | ||||
| chr9:34178952-34179078 | Common:1; Rare:34 | ||||
| chr9:34329228-34329593 | Rare:110 | ||||
| chr9:34458558-34458833 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:34665373-34665660 | Rare:94 | ||||
| chr9:35161786-35162090 | Common:4; Rare:90 | ||||
| chr9:35657841-35658376 | Common:9; Rare:443; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35685437-35685693 | Common:1; Rare:61; Clinvar (benign):4 | ||||
| chr9:35689729-35690091 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35698813-35699046 | Common:1; Rare:64 | ||||
| chr9:35705554-35705810 | Common:1; Rare:61 | ||||
| chr9:35705990-35706290 | Common:2; Rare:70 |