| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322508-18322638 | Common:2; Rare:59 | ||||
| chr11:18396213-18396441 | Rare:75 | ||||
| chr11:18526809-18527072 | Common:2; Rare:119 | ||||
| chr11:18588667-18588965 | Common:4; Rare:87 | ||||
| chr11:18634274-18634590 | Common:3; Rare:111 | ||||
| chr11:18634768-18634836 | Rare:21 | ||||
| chr11:18698520-18698812 | Common:6; Rare:74 | ||||
| chr11:18791521-18791895 | Common:1; Rare:119 | ||||
| chr11:20387450-20387755 | Common:7; Rare:103 | ||||
| chr11:20668639-20669159 | Common:4; Rare:134 | ||||
| chr11:20669435-20669698 | Common:3; Rare:105 | ||||
| chr11:22337877-22337922 | Rare:3 | ||||
| chr11:22624928-22625253 | Common:3; Rare:126; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr11:22625766-22626021 | Common:3; Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:22829321-22829430 | Common:1; Rare:27 |