| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34458568-34458865 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:34612046-34612238 | Common:9; Rare:74 | ||||
| chr9:34620457-34620651 | Common:1; Rare:46 | ||||
| chr9:34637725-34637953 | Rare:67 | ||||
| chr9:34646519-34646804 | Common:1; Rare:91; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34652015-34652217 | Rare:58 | ||||
| chr9:34653734-34653929 | Rare:32 | ||||
| chr9:34665373-34665660 | Rare:94 | ||||
| chr9:34665964-34666177 | Common:2; Rare:56 | ||||
| chr9:35072525-35072965 | Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35103064-35103198 | Common:1; Rare:56 | ||||
| chr9:35161789-35162084 | Common:4; Rare:87 | ||||
| chr9:35162286-35162567 | Rare:61 | ||||
| chr9:35489750-35490144 | Common:3; Rare:121 | ||||
| chr9:35646806-35646867 | Rare:17 |