| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214832-47215094 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:47248791-47248941 | Rare:60 | ||||
| chr11:47269529-47269690 | Common:1; Rare:53 | ||||
| chr11:47269966-47270184 | Common:1; Rare:71 | ||||
| chr11:47553031-47553356 | Common:2; Rare:115 | ||||
| chr11:47565511-47565650 | Common:2; Rare:26 | ||||
| chr11:47578952-47579097 | Rare:74; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642504-47642805 | Rare:108 | ||||
| chr11:47767350-47767642 | Common:1; Rare:72 | ||||
| chr11:57427075-57427207 | Common:1; Rare:43 | ||||
| chr11:57514858-57514915 | Rare:6 | ||||
| chr11:57530684-57530920 | Common:1; Rare:67 | ||||
| chr11:57657527-57657794 | Common:4; Rare:66 | ||||
| chr11:57712175-57712665 | Common:9; Rare:169 | ||||
| chr11:57741177-57741598 | Common:2; Rare:152 |