| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77637587-77637852 | Common:1; Rare:88 | ||||
| chr11:77820841-77821284 | Common:3; Rare:121 | ||||
| chr11:77994600-77994794 | Common:1; Rare:70 | ||||
| chr11:78079579-78079926 | Common:4; Rare:115 | ||||
| chr11:78113890-78114290 | Common:5; Rare:99; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:78139526-78139829 | Common:3; Rare:115; Clinvar:3 | ||||
| chr11:78188588-78188987 | Common:3; Rare:126 | ||||
| chr11:78417697-78417964 | Common:3; Rare:110 | ||||
| chr11:78574759-78574970 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chr11:79440777-79441120 | Common:5; Rare:97 | ||||
| chr11:82900313-82900595 | Common:1; Rare:88 | ||||
| chr11:83071708-83072161 | Common:4; Rare:123 | ||||
| chr11:83193601-83193941 | Common:2; Rare:143 | ||||
| chr11:83285711-83285755 | Common:1; Rare:10 | ||||
| chr11:83285793-83286146 | Common:4; Rare:150 |