| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34646516-34646782 | Common:2; Rare:132; Clinvar:6; Clinvar (pathogenic):3 | ||||
| chr9:34651970-34652250 | Rare:141 | ||||
| chr9:34665220-34665640 | Common:1; Rare:219 | ||||
| chr9:35072464-35072965 | Rare:215; Clinvar:8; Clinvar (benign):2 | ||||
| chr9:35079915-35080095 | Common:8; Rare:75; Clinvar:6; Clinvar (benign):6 | ||||
| chr9:35096556-35096664 | Common:1; Rare:25 | ||||
| chr9:35103039-35103319 | Common:2; Rare:149 | ||||
| chr9:35115830-35116300 | Common:2; Rare:153 | ||||
| chr9:35161785-35162175 | Common:8; Rare:213 | ||||
| chr9:35162352-35162880 | Common:2; Rare:132 | ||||
| chr9:35489922-35490148 | Common:5; Rare:107 | ||||
| chr9:35605136-35605327 | Common:2; Rare:103 | ||||
| chr9:35646700-35647130 | Common:6; Rare:139 | ||||
| chr9:35657883-35658356 | Common:13; Rare:780; Clinvar:70; Clinvar (benign):28; Clinvar (pathogenic):74 | ||||
| chr9:35665165-35665354 | Common:4; Rare:139 |