| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207898-17208093 | Common:2; Rare:77 | ||||
| chr11:17276546-17276822 | Common:5; Rare:78; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18013008-18013261 | Common:5; Rare:80 | ||||
| chr11:18322130-18322306 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322467-18322607 | Common:2; Rare:59 | ||||
| chr11:18526865-18526977 | Rare:52 | ||||
| chr11:18588667-18588815 | Rare:53 | ||||
| chr11:18634332-18634566 | Common:2; Rare:74 | ||||
| chr11:18698653-18698747 | Common:1; Rare:19 | ||||
| chr11:19116939-19117221 | Common:3; Rare:76 | ||||
| chr11:19201956-19202252 | Common:1; Rare:52; Clinvar (benign):5 | ||||
| chr11:20387470-20387747 | Common:5; Rare:93 | ||||
| chr11:24496783-24497095 | Common:2; Rare:83 | ||||
| chr11:27040863-27041009 | Common:1; Rare:24 | ||||
| chr11:27363064-27363289 | Rare:105 |