| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633312-97633426 | Rare:28 | ||||
| chr9:97633467-97633851 | Common:5; Rare:124 | ||||
| chr9:98192630-98192879 | Common:6; Rare:68 | ||||
| chr9:98255578-98255904 | Common:3; Rare:99 | ||||
| chr9:99221964-99222355 | Common:2; Rare:144 | ||||
| chr9:99906570-99906694 | Rare:63 | ||||
| chr9:100098964-100099323 | Common:3; Rare:103; Clinvar:2 | ||||
| chr9:100352897-100353094 | Rare:70 | ||||
| chr9:101398570-101398910 | Common:1; Rare:114 | ||||
| chr9:104093985-104094321 | Common:3; Rare:78 | ||||
| chr9:104747559-104747757 | Rare:50 | ||||
| chr9:105558099-105558170 | Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862997-106863180 | Rare:64 | ||||
| chr9:108934074-108934519 | Common:8; Rare:180; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498246-109498423 | Rare:61 |