| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:2017633-2017739 | Rare:30 | ||||
| chr9:2621379-2621799 | Common:4; Rare:172; Clinvar:1 | ||||
| chr9:2621837-2622198 | Common:6; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
| chr9:2844043-2844359 | Common:5; Rare:124 | ||||
| chr9:3525771-3526119 | Common:1; Rare:130 | ||||
| chr9:3526425-3526521 | Common:1; Rare:50 | ||||
| chr9:4662262-4662323 | Common:1; Rare:20 | ||||
| chr9:4679428-4679840 | Common:1; Rare:182 | ||||
| chr9:4741071-4741433 | Common:6; Rare:172 | ||||
| chr9:4741770-4741996 | Common:4; Rare:74 | ||||
| chr9:4742007-4742043 | Rare:9 | ||||
| chr9:4792607-4793054 | Common:3; Rare:161 | ||||
| chr9:4984720-4985090 | Common:1; Rare:137 | ||||
| chr9:5437780-5438017 | Common:1; Rare:82 | ||||
| chr9:5450411-5450593 | Common:5; Rare:72 |