| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72016220-72016521 | Common:2; Rare:77 | ||||
| chr11:72018398-72018821 | Common:3; Rare:105 | ||||
| chr11:72019493-72019853 | Common:1; Rare:81 | ||||
| chr11:72021202-72021536 | Common:1; Rare:66 | ||||
| chr11:72195179-72195644 | Common:4; Rare:126; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:72229488-72229692 | Common:1; Rare:70; Clinvar (pathogenic):1 | ||||
| chr11:72230001-72230183 | Common:1; Rare:52 | ||||
| chr11:72691474-72691502 | Rare:4 | ||||
| chr11:72712228-72712503 | Common:1; Rare:95 | ||||
| chr11:72738974-72739207 | Common:3; Rare:33 | ||||
| chr11:72825965-72826242 | Common:2; Rare:72 | ||||
| chr11:73200406-73200468 | Common:1; Rare:12 | ||||
| chr11:73309246-73309513 | Common:1; Rare:98 | ||||
| chr11:73309725-73309869 | Common:1; Rare:69 | ||||
| chr11:74845219-74845539 | Common:2; Rare:71 |