| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66347974-66348221 | Common:1; Rare:102 | ||||
| chr11:66438556-66438605 | Rare:17 | ||||
| chr11:66438735-66438856 | Common:1; Rare:42 | ||||
| chr11:66466677-66466911 | Rare:66 | ||||
| chr11:66479944-66480022 | Rare:15 | ||||
| chr11:66480107-66480506 | Common:3; Rare:100 | ||||
| chr11:66480624-66480787 | Common:1; Rare:40 | ||||
| chr11:66510545-66510712 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr11:66545948-66546341 | Common:5; Rare:107 | ||||
| chr11:66592995-66593288 | Common:1; Rare:104 | ||||
| chr11:66616118-66616291 | Rare:40 | ||||
| chr11:66616319-66616681 | Common:2; Rare:112 | ||||
| chr11:66616973-66617164 | Common:1; Rare:75 | ||||
| chr11:66638356-66638735 | Common:4; Rare:173 | ||||
| chr11:66677786-66678173 | Common:1; Rare:135 |