| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46120491-46120967 | Rare:95 | ||||
| chr11:46121354-46121614 | Rare:71 | ||||
| chr11:46347244-46347487 | Common:2; Rare:75 | ||||
| chr11:46380669-46380968 | Common:1; Rare:81 | ||||
| chr11:46381501-46381761 | Common:1; Rare:63 | ||||
| chr11:46594005-46594160 | Common:1; Rare:31 | ||||
| chr11:46700565-46700775 | Common:1; Rare:52 | ||||
| chr11:46700788-46701081 | Common:3; Rare:73 | ||||
| chr11:46846224-46846482 | Common:1; Rare:73 | ||||
| chr11:46918510-46918759 | Common:3; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:46936583-46936786 | Common:2; Rare:52 | ||||
| chr11:47176836-47177154 | Common:1; Rare:131 | ||||
| chr11:47177290-47177660 | Rare:64 | ||||
| chr11:47185288-47185688 | Common:4; Rare:131 | ||||
| chr11:47186373-47186560 | Rare:54 |