| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:114587453-114587910 | Common:4; Rare:166 | ||||
| chr9:116687203-116687372 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:117703929-117704464 | Common:2; Rare:101 | ||||
| chr9:120714452-120714726 | Common:2; Rare:95 | ||||
| chr9:120793242-120793543 | Common:2; Rare:110 | ||||
| chr9:120842905-120843274 | Common:1; Rare:117 | ||||
| chr9:120843290-120843378 | Common:1; Rare:26 | ||||
| chr9:120868827-120869117 | Common:2; Rare:63 | ||||
| chr9:120877125-120877493 | Common:3; Rare:118 | ||||
| chr9:120929108-120929183 | Common:1; Rare:17 | ||||
| chr9:121074819-121074983 | Rare:82 | ||||
| chr9:121075109-121075409 | Rare:65 | ||||
| chr9:121121619-121121860 | Rare:67 | ||||
| chr9:121201794-121202168 | Common:2; Rare:115 | ||||
| chr9:121268010-121268207 | Common:1; Rare:67 |