| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108223971-108224082 | Rare:29 | ||||
| chr11:108467501-108467658 | Common:3; Rare:56 | ||||
| chr11:108664788-108665120 | Common:5; Rare:126 | ||||
| chr11:110092850-110093171 | Common:4; Rare:108 | ||||
| chr11:110712363-110712633 | Common:2; Rare:93 | ||||
| chr11:111299673-111299752 | Common:2; Rare:18 | ||||
| chr11:111541417-111541572 | Common:2; Rare:27 | ||||
| chr11:111602153-111602671 | Common:1; Rare:155 | ||||
| chr11:111735803-111736045 | Rare:49 | ||||
| chr11:111766020-111766463 | Common:6; Rare:206 | ||||
| chr11:111766678-111766814 | Rare:32 | ||||
| chr11:111836219-111836492 | Common:1; Rare:58; Clinvar (benign):2 | ||||
| chr11:111845606-111845797 | Rare:27 | ||||
| chr11:111871243-111871378 | Common:1; Rare:44; Clinvar:1 | ||||
| chr11:111878666-111879016 | Common:2; Rare:113 |