| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:78079635-78079933 | Common:2; Rare:102 | ||||
| chr11:78139587-78139845 | Common:3; Rare:97; Clinvar:2 | ||||
| chr11:78188586-78188832 | Common:2; Rare:72 | ||||
| chr11:78417724-78418039 | Common:3; Rare:132 | ||||
| chr11:78574773-78574972 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr11:82900400-82900643 | Common:1; Rare:65 | ||||
| chr11:83071719-83072130 | Common:4; Rare:110 | ||||
| chr11:83193617-83193786 | Common:1; Rare:79 | ||||
| chr11:83285734-83286130 | Common:4; Rare:167 | ||||
| chr11:83286331-83286506 | Rare:43 | ||||
| chr11:85627796-85628062 | Common:1; Rare:54 | ||||
| chr11:85628324-85628688 | Common:7; Rare:122 | ||||
| chr11:85647851-85648089 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:86244971-86245269 | Common:1; Rare:132 | ||||
| chr11:86671805-86672262 | Common:2; Rare:110 |