| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93741464-93741728 | Common:5; Rare:100 | ||||
| chr11:93784189-93784384 | Common:3; Rare:56 | ||||
| chr11:94128782-94129293 | Common:5; Rare:169 | ||||
| chr11:94493789-94494058 | Common:5; Rare:78; Clinvar (benign):1 | ||||
| chr11:94543792-94543965 | Common:3; Rare:41 | ||||
| chr11:94767946-94768553 | Common:3; Rare:167 | ||||
| chr11:94973525-94973733 | Rare:64 | ||||
| chr11:95067448-95067590 | Rare:58 | ||||
| chr11:95089731-95089930 | Common:3; Rare:87 | ||||
| chr11:95789459-95789853 | Common:3; Rare:183 | ||||
| chr11:95790359-95790598 | Common:1; Rare:91 | ||||
| chr11:95923829-95924207 | Common:2; Rare:163; Clinvar:6; Clinvar (benign):5 | ||||
| chr11:96389857-96390043 | Common:1; Rare:75 | ||||
| chr11:101127523-101127858 | Common:3; Rare:147 | ||||
| chr11:101583464-101583575 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 |