| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77820532-77820594 | Rare:21 | ||||
| chr11:77820815-77821254 | Common:2; Rare:121 | ||||
| chr11:78079577-78079956 | Common:4; Rare:125 | ||||
| chr11:78139450-78139756 | Common:1; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:78188574-78189016 | Common:3; Rare:139 | ||||
| chr11:78574764-78574940 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr11:82900299-82900595 | Common:1; Rare:92 | ||||
| chr11:83071701-83072145 | Common:4; Rare:118 | ||||
| chr11:83193598-83193843 | Common:1; Rare:110 | ||||
| chr11:83285682-83285726 | Rare:8 | ||||
| chr11:83285868-83286136 | Common:3; Rare:120 | ||||
| chr11:85627303-85627589 | Rare:47 | ||||
| chr11:85628332-85628687 | Common:7; Rare:117 | ||||
| chr11:85628979-85629203 | Rare:65 | ||||
| chr11:85647926-85648124 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):3 |