| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65614192-65614348 | Rare:36 | ||||
| chr11:65662890-65663116 | Common:1; Rare:55 | ||||
| chr11:65711869-65712042 | Rare:53 | ||||
| chr11:65712210-65712276 | Rare:20 | ||||
| chr11:65856912-65857356 | Common:4; Rare:128 | ||||
| chr11:65859462-65859694 | Rare:59 | ||||
| chr11:65860366-65860466 | Common:1; Rare:33 | ||||
| chr11:65860518-65860754 | Common:1; Rare:69 | ||||
| chr11:65873577-65873700 | Common:1; Rare:43 | ||||
| chr11:65888392-65888686 | Common:1; Rare:103 | ||||
| chr11:65900370-65900528 | Common:1; Rare:28 | ||||
| chr11:65961541-65961764 | Rare:76 | ||||
| chr11:66002102-66002392 | Common:3; Rare:87; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:66002448-66002824 | Common:1; Rare:102; Clinvar:1 | ||||
| chr11:66257602-66257794 | Rare:48 |