| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61429892-61430170 | Common:1; Rare:122; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792555-61792955 | Common:6; Rare:114 | ||||
| chr11:61967116-61967571 | Common:2; Rare:149; Clinvar:1 | ||||
| chr11:61967576-61967806 | Common:2; Rare:87; Clinvar:3 | ||||
| chr11:62545170-62545271 | Rare:17 | ||||
| chr11:62545566-62546140 | Common:1; Rare:128 | ||||
| chr11:62546659-62546925 | Common:1; Rare:82 | ||||
| chr11:62591481-62591823 | Rare:117 | ||||
| chr11:62601220-62601304 | Rare:19 | ||||
| chr11:62601615-62601712 | Rare:26 | ||||
| chr11:62601778-62602257 | Common:2; Rare:122 | ||||
| chr11:62611540-62611837 | Rare:74 | ||||
| chr11:62646563-62646877 | Common:2; Rare:118; Clinvar (pathogenic):1 | ||||
| chr11:62653262-62653504 | Common:1; Rare:72 | ||||
| chr11:62665139-62665458 | Common:6; Rare:149 |