| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95875975-95876032 | Common:3; Rare:28 | ||||
| chr9:96383654-96383777 | Common:1; Rare:40 | ||||
| chr9:96566804-96567006 | Common:1; Rare:61 | ||||
| chr9:96655307-96655431 | Rare:29 | ||||
| chr9:96778040-96778360 | Common:2; Rare:88 | ||||
| chr9:97633302-97633825 | Common:6; Rare:160 | ||||
| chr9:97697299-97697461 | Common:1; Rare:88; Clinvar:5 | ||||
| chr9:97922460-97922583 | Common:3; Rare:64 | ||||
| chr9:97983004-97983405 | Common:1; Rare:159 | ||||
| chr9:98056578-98056750 | Common:1; Rare:54 | ||||
| chr9:98255598-98255830 | Common:3; Rare:69 | ||||
| chr9:99221898-99222355 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99821750-99821988 | Rare:63 | ||||
| chr9:99906601-99906713 | Rare:51 | ||||
| chr9:100098952-100099305 | Common:3; Rare:99; Clinvar:1 |