| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33736396-33736607 | Common:1; Rare:66 | ||||
| chr11:33774457-33774710 | Common:2; Rare:97 | ||||
| chr11:34051418-34051753 | Rare:113 | ||||
| chr11:34052036-34052444 | Common:5; Rare:177 | ||||
| chr11:34052571-34052971 | Common:4; Rare:194 | ||||
| chr11:34053212-34053703 | Common:2; Rare:216 | ||||
| chr11:34105458-34105743 | Common:4; Rare:94 | ||||
| chr11:34105762-34106162 | Common:3; Rare:99 | ||||
| chr11:34438745-34438921 | Rare:54 | ||||
| chr11:34916030-34916681 | Common:14; Rare:249; Clinvar:6; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:35419202-35420522 | Common:8; Rare:396 | ||||
| chr11:35617920-35618045 | Rare:21 | ||||
| chr11:35618207-35618465 | Common:3; Rare:77 | ||||
| chr11:35662686-35662913 | Common:2; Rare:67 | ||||
| chr11:35943940-35944113 | Common:2; Rare:58 |