| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:214678-214879 | Common:4; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215076-215220 | Common:3; Rare:78; Clinvar (benign):1 | ||||
| chr9:470142-470379 | Common:15; Rare:104 | ||||
| chr9:504369-504739 | Common:4; Rare:180 | ||||
| chr9:2015073-2015396 | Common:3; Rare:93 | ||||
| chr9:2016964-2017183 | Rare:55 | ||||
| chr9:2017633-2017745 | Rare:31 | ||||
| chr9:2621983-2622175 | Common:6; Rare:68; Clinvar:8; Clinvar (benign):3 | ||||
| chr9:2844034-2844357 | Common:5; Rare:127 | ||||
| chr9:3525958-3526106 | Common:1; Rare:62 | ||||
| chr9:3526405-3526536 | Common:4; Rare:71 | ||||
| chr9:4662017-4662338 | Common:5; Rare:107 | ||||
| chr9:4679423-4679791 | Common:1; Rare:161 | ||||
| chr9:4741080-4741406 | Common:6; Rare:154 | ||||
| chr9:4792674-4793002 | Common:2; Rare:127 |