| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112379794-112380163 | Common:4; Rare:144 | ||||
| chr9:113056657-113056909 | Common:1; Rare:81; Clinvar:1 | ||||
| chr9:113221230-113221603 | Common:1; Rare:120 | ||||
| chr9:113275359-113275734 | Common:5; Rare:119; Clinvar (pathogenic):1 | ||||
| chr9:113376914-113377124 | Common:8; Rare:70 | ||||
| chr9:113410281-113410720 | Common:3; Rare:130 | ||||
| chr9:114505465-114505633 | Common:1; Rare:48 | ||||
| chr9:114587598-114587881 | Common:2; Rare:103 | ||||
| chr9:115118155-115118456 | Rare:70 | ||||
| chr9:116687171-116687364 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793248-120793534 | Common:1; Rare:104 | ||||
| chr9:120842890-120843251 | Common:1; Rare:119 | ||||
| chr9:120868827-120869090 | Common:2; Rare:57 | ||||
| chr9:120877144-120877458 | Common:3; Rare:98 | ||||
| chr9:121074837-121074992 | Rare:78 |