| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111525065-111525226 | Common:3; Rare:52 | ||||
| chr9:111794935-111795016 | Common:1; Rare:13 | ||||
| chr9:112379880-112380159 | Common:1; Rare:116 | ||||
| chr9:112718033-112718157 | Common:2; Rare:33 | ||||
| chr9:113221262-113221610 | Rare:109 | ||||
| chr9:113275380-113275728 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:113401248-113401556 | Common:6; Rare:114; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410317-113410667 | Common:2; Rare:101 | ||||
| chr9:114387983-114388104 | Common:1; Rare:42 | ||||
| chr9:116687187-116687364 | Common:4; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793248-120793543 | Common:2; Rare:109 | ||||
| chr9:120842897-120843251 | Common:1; Rare:116 | ||||
| chr9:120868831-120869060 | Common:2; Rare:48 | ||||
| chr9:120877177-120877482 | Common:2; Rare:102 | ||||
| chr9:121074851-121074989 | Rare:72 |