| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:116687235-116687370 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793255-120793551 | Common:2; Rare:110 | ||||
| chr9:120842905-120843222 | Common:1; Rare:104 | ||||
| chr9:120877153-120877482 | Common:3; Rare:108 | ||||
| chr9:121074851-121074981 | Rare:65 | ||||
| chr9:121201832-121202149 | Common:2; Rare:93 | ||||
| chr9:121370203-121370534 | Common:2; Rare:95 | ||||
| chr9:122264542-122264691 | Common:2; Rare:34 | ||||
| chr9:122264737-122264928 | Common:2; Rare:55 | ||||
| chr9:122828486-122828770 | Rare:84 | ||||
| chr9:122905233-122905566 | Common:2; Rare:124 | ||||
| chr9:122931482-122931701 | Common:3; Rare:45 | ||||
| chr9:124861883-124862145 | Common:1; Rare:117 | ||||
| chr9:124940969-124941142 | Common:3; Rare:61 | ||||
| chr9:125189733-125189860 | Rare:83 |