| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61816760-61816981 | Rare:65 | ||||
| chr11:61967089-61967806 | Common:4; Rare:239; Clinvar:4 | ||||
| chr11:62337197-62337549 | Common:5; Rare:92 | ||||
| chr11:62545188-62545265 | Rare:15 | ||||
| chr11:62545578-62546022 | Common:1; Rare:101 | ||||
| chr11:62546646-62547159 | Common:1; Rare:143 | ||||
| chr11:62591489-62591857 | Rare:124 | ||||
| chr11:62601225-62601294 | Rare:15 | ||||
| chr11:62601640-62601869 | Rare:74 | ||||
| chr11:62611540-62611860 | Rare:78 | ||||
| chr11:62646560-62646817 | Common:1; Rare:105; Clinvar (pathogenic):1 | ||||
| chr11:62653257-62653487 | Common:1; Rare:72 | ||||
| chr11:62665140-62665470 | Common:6; Rare:154 | ||||
| chr11:62678864-62679184 | Rare:108 | ||||
| chr11:62706201-62706405 | Common:3; Rare:77; Clinvar (benign):6 |