| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46701008-46701109 | Common:1; Rare:46 | ||||
| chr11:46719128-46719273 | Rare:37 | ||||
| chr11:46845698-46845953 | Common:1; Rare:52 | ||||
| chr11:46845975-46846097 | Rare:23 | ||||
| chr11:46846120-46846454 | Common:1; Rare:104 | ||||
| chr11:46918306-46918368 | Rare:15; Clinvar:1 | ||||
| chr11:46918502-46918691 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:46936624-46937015 | Common:2; Rare:103 | ||||
| chr11:46937047-46937095 | Rare:6 | ||||
| chr11:47176749-47177166 | Common:1; Rare:182 | ||||
| chr11:47177328-47177374 | Rare:6 | ||||
| chr11:47177425-47177631 | Rare:38 | ||||
| chr11:47185363-47185707 | Common:2; Rare:69 | ||||
| chr11:47185729-47186273 | Common:1; Rare:112 | ||||
| chr11:47186327-47186615 | Rare:72 |