| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113376921-113377118 | Common:7; Rare:67 | ||||
| chr9:113410286-113410741 | Common:4; Rare:143 | ||||
| chr9:114587453-114587863 | Common:4; Rare:150 | ||||
| chr9:116687228-116687346 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:120793248-120793543 | Common:2; Rare:109 | ||||
| chr9:120842905-120843121 | Common:1; Rare:78 | ||||
| chr9:121074819-121074981 | Rare:81 | ||||
| chr9:121075129-121075289 | Rare:35 | ||||
| chr9:121201814-121202151 | Common:2; Rare:106 | ||||
| chr9:121268068-121268207 | Common:1; Rare:45 | ||||
| chr9:121370183-121370527 | Common:2; Rare:103 | ||||
| chr9:122159722-122159953 | Rare:81 | ||||
| chr9:122264774-122264927 | Common:2; Rare:45 | ||||
| chr9:122931482-122931677 | Common:3; Rare:36 | ||||
| chr9:122940830-122941062 | Common:2; Rare:92 |