| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18394278-18394658 | Common:1; Rare:140; Clinvar (benign):1 | ||||
| chr11:18526841-18526977 | Rare:66 | ||||
| chr11:18588656-18588941 | Common:4; Rare:95 | ||||
| chr11:18634332-18634566 | Common:2; Rare:74 | ||||
| chr11:20363657-20363753 | Common:1; Rare:21 | ||||
| chr11:20364041-20364392 | Common:6; Rare:107 | ||||
| chr11:20387496-20387773 | Common:4; Rare:86 | ||||
| chr11:22625499-22625609 | Rare:52; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626011 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829359-22829422 | Common:1; Rare:18 | ||||
| chr11:22829693-22829933 | Common:3; Rare:91 | ||||
| chr11:27363058-27363359 | Rare:132 | ||||
| chr11:27506737-27506875 | Common:1; Rare:60 | ||||
| chr11:28108115-28108421 | Common:1; Rare:94 | ||||
| chr11:30322971-30323169 | Common:1; Rare:57 |