| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65890453-65890711 | Common:4; Rare:86 | ||||
| chr11:65919528-65919846 | Common:1; Rare:102 | ||||
| chr11:66001590-66001839 | Common:3; Rare:42 | ||||
| chr11:66002128-66002402 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:66002465-66002795 | Common:1; Rare:89; Clinvar:1 | ||||
| chr11:66257500-66257768 | Rare:64 | ||||
| chr11:66268810-66268865 | Common:2; Rare:18 | ||||
| chr11:66289104-66289393 | Rare:65 | ||||
| chr11:66480226-66480446 | Common:1; Rare:59 | ||||
| chr11:66546019-66546134 | Rare:27 | ||||
| chr11:66616389-66616657 | Common:1; Rare:79 | ||||
| chr11:66638393-66638708 | Common:3; Rare:138 | ||||
| chr11:66744666-66744896 | Common:2; Rare:87 | ||||
| chr11:66843317-66843455 | Common:5; Rare:72 | ||||
| chr11:67239886-67240183 | Rare:64 |