| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:76379992-76380330 | Common:1; Rare:64 | ||||
| chr11:76408191-76408281 | Common:1; Rare:13 | ||||
| chr11:76445600-76446030 | Common:3; Rare:84 | ||||
| chr11:76792527-76792689 | Rare:27 | ||||
| chr11:76807123-76807331 | Common:2; Rare:38 | ||||
| chr11:76807422-76807708 | Common:8; Rare:77 | ||||
| chr11:76823715-76823896 | Rare:31 | ||||
| chr11:77065906-77066103 | Common:1; Rare:41 | ||||
| chr11:77147948-77148307 | Common:1; Rare:106; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:77638427-77638502 | Rare:13 | ||||
| chr11:77644670-77644829 | Rare:28 | ||||
| chr11:77819431-77819714 | Rare:70 | ||||
| chr11:78040068-78040230 | Rare:28 | ||||
| chr11:78040526-78040610 | Common:1; Rare:14 | ||||
| chr11:78140575-78140603 | Rare:6 |