| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77994589-77995175 | Common:3; Rare:177 | ||||
| chr11:78023090-78023490 | Common:11; Rare:214 | ||||
| chr11:78046190-78046610 | Common:3; Rare:88 | ||||
| chr11:78079745-78080046 | Common:2; Rare:89 | ||||
| chr11:78112485-78112832 | Common:4; Rare:113; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:78138889-78139289 | Common:4; Rare:115 | ||||
| chr11:78139547-78139854 | Common:3; Rare:116; Clinvar:3 | ||||
| chr11:78188586-78188830 | Common:2; Rare:72 | ||||
| chr11:78416818-78417560 | Common:13; Rare:310 | ||||
| chr11:78417721-78418047 | Common:3; Rare:133 | ||||
| chr11:78574172-78574572 | Common:3; Rare:131; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:78574764-78574986 | Common:2; Rare:86; Clinvar (benign):1 | ||||
| chr11:78575160-78575289 | Rare:25 | ||||
| chr11:78962173-78962570 | Common:4; Rare:85 | ||||
| chr11:79438335-79439391 | Common:11; Rare:298 |