| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65279723-65280123 | Common:6; Rare:83 | ||||
| chr11:65314558-65314982 | Common:6; Rare:597 | ||||
| chr11:65315181-65315673 | Common:7; Rare:231 | ||||
| chr11:65333410-65334070 | Common:7; Rare:699 | ||||
| chr11:65334148-65334548 | Common:3; Rare:164 | ||||
| chr11:65354394-65354794 | Common:3; Rare:267 | ||||
| chr11:65381620-65382258 | Common:15; Rare:366 | ||||
| chr11:65382321-65382880 | Common:13; Rare:419 | ||||
| chr11:65386375-65386779 | Common:3; Rare:515 | ||||
| chr11:65503622-65504022 | Common:1; Rare:211 | ||||
| chr11:65503942-65504471 | Common:4; Rare:389 | ||||
| chr11:65524758-65525222 | Rare:400 | ||||
| chr11:65525180-65526266 | Common:4; Rare:506; Clinvar (pathogenic):2 | ||||
| chr11:65540010-65540626 | Common:4; Rare:316; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65540535-65541226 | Common:24; Rare:836; Clinvar:2; Clinvar (benign):3 |