| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108121384-108121608 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108222594-108223128 | Common:1; Rare:170; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108467469-108467605 | Common:1; Rare:52 | ||||
| chr11:108664788-108665156 | Common:6; Rare:146 | ||||
| chr11:110296478-110296760 | Common:1; Rare:131; Clinvar:8 | ||||
| chr11:111299643-111299779 | Common:2; Rare:33 | ||||
| chr11:111514728-111514892 | Common:1; Rare:67 | ||||
| chr11:111541508-111541558 | Common:1; Rare:14 | ||||
| chr11:111602237-111602572 | Common:1; Rare:112 | ||||
| chr11:111766338-111766426 | Rare:48 | ||||
| chr11:111871254-111871378 | Rare:40; Clinvar:1 | ||||
| chr11:111878700-111878950 | Common:2; Rare:60 | ||||
| chr11:111879147-111879554 | Common:1; Rare:126 | ||||
| chr11:111912611-111912757 | Common:1; Rare:36 | ||||
| chr11:111913126-111913276 | Rare:42 |