| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:2017483-2017791 | Rare:88 | ||||
| chr9:2621860-2622218 | Common:7; Rare:126; Clinvar:8; Clinvar (benign):5 | ||||
| chr9:2844034-2844334 | Common:5; Rare:110 | ||||
| chr9:3525966-3526115 | Common:1; Rare:69 | ||||
| chr9:3526409-3526719 | Common:6; Rare:147 | ||||
| chr9:4662227-4662343 | Common:2; Rare:43 | ||||
| chr9:4679423-4679891 | Common:1; Rare:209 | ||||
| chr9:4741026-4741381 | Common:5; Rare:173 | ||||
| chr9:4792685-4793110 | Common:2; Rare:159 | ||||
| chr9:4984741-4985101 | Common:1; Rare:131 | ||||
| chr9:5437803-5437982 | Common:1; Rare:65 | ||||
| chr9:5450437-5450596 | Common:5; Rare:61 | ||||
| chr9:5628892-5629215 | Common:1; Rare:158 | ||||
| chr9:6015593-6015719 | Rare:56 | ||||
| chr9:6757100-6757402 | Common:3; Rare:81 |