| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221879-99222365 | Common:2; Rare:200; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:99821923-99822046 | Rare:19 | ||||
| chr9:99906561-99906728 | Rare:73 | ||||
| chr9:100098915-100099314 | Common:3; Rare:111; Clinvar:2 | ||||
| chr9:100352822-100353094 | Rare:99 | ||||
| chr9:100426614-100426716 | Rare:19 | ||||
| chr9:100427028-100427384 | Common:7; Rare:128 | ||||
| chr9:101398570-101398907 | Common:1; Rare:113 | ||||
| chr9:104093985-104094354 | Common:4; Rare:90 | ||||
| chr9:105447976-105448144 | Common:2; Rare:59 | ||||
| chr9:105558040-105558168 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862572-106862776 | Common:1; Rare:54 | ||||
| chr9:106862900-106863191 | Rare:87 | ||||
| chr9:107284000-107284307 | Common:1; Rare:88 | ||||
| chr9:107284592-107284869 | Common:2; Rare:61 |