| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45917823-45917983 | Rare:47; Clinvar:1 | ||||
| chr11:45918018-45918253 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr11:45918787-45918925 | Rare:40 | ||||
| chr11:46119315-46120002 | Common:14; Rare:227 | ||||
| chr11:46120510-46121020 | Rare:96 | ||||
| chr11:46121342-46121610 | Rare:70 | ||||
| chr11:46315131-46315392 | Common:1; Rare:47 | ||||
| chr11:46347218-46347577 | Common:2; Rare:112 | ||||
| chr11:46380722-46380982 | Common:1; Rare:68 | ||||
| chr11:46593516-46593916 | Rare:161 | ||||
| chr11:46593997-46594188 | Common:2; Rare:36 | ||||
| chr11:46617070-46617329 | Rare:70 | ||||
| chr11:46617440-46617610 | Common:3; Rare:66 | ||||
| chr11:46617733-46618133 | Common:2; Rare:131 | ||||
| chr11:46700527-46700775 | Common:1; Rare:61 |