| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66479910-66480124 | Common:1; Rare:37 | ||||
| chr11:66480126-66480484 | Common:3; Rare:96 | ||||
| chr11:66510519-66510703 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66545730-66545826 | Common:1; Rare:22 | ||||
| chr11:66545917-66546328 | Common:5; Rare:107 | ||||
| chr11:66592739-66592961 | Rare:79 | ||||
| chr11:66593005-66593272 | Common:1; Rare:95 | ||||
| chr11:66616111-66616297 | Rare:42 | ||||
| chr11:66616320-66616691 | Common:2; Rare:116 | ||||
| chr11:66616798-66617186 | Common:1; Rare:126 | ||||
| chr11:66638278-66638830 | Common:4; Rare:228 | ||||
| chr11:66639098-66639157 | Rare:14 | ||||
| chr11:66677560-66678225 | Common:1; Rare:212 | ||||
| chr11:66728349-66728496 | Rare:40 | ||||
| chr11:66744472-66745015 | Common:5; Rare:164 |