| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64359083-64359257 | Common:1; Rare:44 | ||||
| chr11:64778399-64778584 | Common:1; Rare:108 | ||||
| chr11:64810521-64810821 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65013587-65013697 | Rare:21 | ||||
| chr11:65014019-65014257 | Rare:61 | ||||
| chr11:65083972-65084310 | Common:2; Rare:111 | ||||
| chr11:65096107-65096245 | Common:1; Rare:38 | ||||
| chr11:65134480-65134579 | Common:1; Rare:25 | ||||
| chr11:65181243-65181378 | Common:1; Rare:37 | ||||
| chr11:65181879-65181972 | Rare:16 | ||||
| chr11:65261739-65262010 | Common:4; Rare:81 | ||||
| chr11:65314717-65314884 | Rare:57 | ||||
| chr11:65333624-65333881 | Common:1; Rare:112 | ||||
| chr11:65386495-65386696 | Rare:65 | ||||
| chr11:65570285-65570504 | Rare:82 |