| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:116687228-116687346 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:117704207-117704399 | Common:1; Rare:37 | ||||
| chr9:120580118-120580360 | Common:1; Rare:79; Clinvar:5 | ||||
| chr9:120793248-120793534 | Common:1; Rare:104 | ||||
| chr9:120842905-120843111 | Common:1; Rare:73 | ||||
| chr9:120876375-120876589 | Common:2; Rare:63 | ||||
| chr9:120877159-120877546 | Common:2; Rare:131 | ||||
| chr9:120929123-120929202 | Common:2; Rare:17 | ||||
| chr9:121074258-121074577 | Common:1; Rare:74 | ||||
| chr9:121074775-121075000 | Rare:108 | ||||
| chr9:121201838-121202158 | Common:2; Rare:91 | ||||
| chr9:121370240-121370446 | Common:1; Rare:51 | ||||
| chr9:122264713-122264922 | Common:3; Rare:57 | ||||
| chr9:122905281-122905552 | Common:2; Rare:108 | ||||
| chr9:122913309-122913422 | Common:2; Rare:28 |