| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20363659-20364211 | Common:10; Rare:124 | ||||
| chr11:20387382-20387801 | Common:8; Rare:137 | ||||
| chr11:22625507-22625609 | Rare:50; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625807-22626006 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829343-22829440 | Common:1; Rare:27 | ||||
| chr11:26572061-26572466 | Rare:68 | ||||
| chr11:26993935-26994178 | Common:2; Rare:40 | ||||
| chr11:27040779-27041038 | Common:2; Rare:49 | ||||
| chr11:27363128-27363334 | Rare:86 | ||||
| chr11:27506729-27506875 | Common:1; Rare:68 | ||||
| chr11:28108134-28108431 | Common:1; Rare:90 | ||||
| chr11:30322971-30323202 | Common:2; Rare:65 | ||||
| chr11:30584028-30584175 | Rare:34 | ||||
| chr11:30584194-30584582 | Common:17; Rare:73 | ||||
| chr11:30584679-30584813 | Rare:26 |