| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108664777-108665133 | Common:5; Rare:136 | ||||
| chr11:110093228-110093366 | Common:5; Rare:39 | ||||
| chr11:110296912-110297120 | Rare:49 | ||||
| chr11:110429809-110429991 | Common:2; Rare:54 | ||||
| chr11:110430010-110430290 | Common:5; Rare:63 | ||||
| chr11:111602320-111602472 | Common:1; Rare:52 | ||||
| chr11:111766330-111766483 | Common:2; Rare:89 | ||||
| chr11:111871243-111871677 | Common:4; Rare:140; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:111878660-111879011 | Common:2; Rare:111 | ||||
| chr11:111879157-111879289 | Rare:53 | ||||
| chr11:111879427-111879559 | Common:1; Rare:45 | ||||
| chr11:111918768-111918921 | Common:1; Rare:29 | ||||
| chr11:111926820-111927350 | Common:12; Rare:106 | ||||
| chr11:111936910-111937220 | Common:10; Rare:79 | ||||
| chr11:112024806-112025168 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 |