| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:114610940-114611410 | Common:2; Rare:108 | ||||
| chr9:114611593-114611993 | Common:3; Rare:130 | ||||
| chr9:116153371-116154161 | Common:6; Rare:238 | ||||
| chr9:116687185-116687427 | Common:4; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:119369235-119369721 | Common:4; Rare:179 | ||||
| chr9:120580099-120580412 | Common:1; Rare:98; Clinvar:5 | ||||
| chr9:120714451-120714752 | Common:2; Rare:102 | ||||
| chr9:120793345-120793598 | Common:5; Rare:97 | ||||
| chr9:120842920-120843051 | Common:1; Rare:38 | ||||
| chr9:120876360-120876850 | Common:5; Rare:300 | ||||
| chr9:120877113-120877263 | Common:4; Rare:56 | ||||
| chr9:120877325-120877586 | Common:1; Rare:98 | ||||
| chr9:121074889-121075013 | Rare:62 | ||||
| chr9:121075109-121075315 | Rare:51 | ||||
| chr9:121121632-121121847 | Rare:58 |