| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57335740-57335953 | Common:4; Rare:49 | ||||
| chr11:57427078-57427424 | Common:2; Rare:77 | ||||
| chr11:57667755-57668081 | Common:4; Rare:98 | ||||
| chr11:57712192-57712618 | Common:9; Rare:142 | ||||
| chr11:57741283-57741598 | Common:1; Rare:117 | ||||
| chr11:58578340-58578499 | Common:2; Rare:58 | ||||
| chr11:59106881-59107193 | Common:3; Rare:102 | ||||
| chr11:59142711-59142864 | Rare:21 | ||||
| chr11:60841918-60842120 | Common:2; Rare:75 | ||||
| chr11:60913835-60914232 | Common:1; Rare:83 | ||||
| chr11:61333045-61333240 | Rare:64 | ||||
| chr11:61361870-61361950 | Rare:16 | ||||
| chr11:61362269-61362407 | Common:1; Rare:38; Clinvar:6 | ||||
| chr11:61392502-61392649 | Common:2; Rare:49; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429920-61430144 | Common:1; Rare:101; Clinvar (benign):2 |