| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:76444645-76444731 | Rare:24 | ||||
| chr11:76444764-76445059 | Common:1; Rare:61 | ||||
| chr11:76782239-76782397 | Rare:24 | ||||
| chr11:76783029-76783397 | Common:10; Rare:118 | ||||
| chr11:76783979-76784186 | Common:4; Rare:53 | ||||
| chr11:77473541-77473673 | Common:1; Rare:44 | ||||
| chr11:77637589-77637855 | Common:1; Rare:89 | ||||
| chr11:77820840-77821284 | Common:3; Rare:121 | ||||
| chr11:78023211-78023531 | Common:4; Rare:76 | ||||
| chr11:78079577-78079926 | Common:4; Rare:117 | ||||
| chr11:78139072-78139163 | Common:1; Rare:19 | ||||
| chr11:78139502-78139853 | Common:3; Rare:130; Clinvar:3 | ||||
| chr11:78188586-78188957 | Common:3; Rare:115 | ||||
| chr11:78574506-78574530 | Common:1; Rare:9; Clinvar (benign):4 | ||||
| chr11:78574704-78574972 | Common:2; Rare:107; Clinvar (benign):1 |