| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65720468-65720579 | Common:1; Rare:62 | ||||
| chr11:65856996-65857319 | Common:4; Rare:98 | ||||
| chr11:65860341-65860748 | Common:3; Rare:128 | ||||
| chr11:65872735-65872937 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:65888425-65888686 | Common:1; Rare:91 | ||||
| chr11:65890422-65890696 | Common:5; Rare:82 | ||||
| chr11:65920158-65920443 | Common:1; Rare:84 | ||||
| chr11:65961517-65961748 | Common:1; Rare:79 | ||||
| chr11:66002097-66002369 | Common:3; Rare:84; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:66002456-66002818 | Common:1; Rare:101; Clinvar:1 | ||||
| chr11:66257568-66257785 | Rare:54 | ||||
| chr11:66258397-66258522 | Rare:29 | ||||
| chr11:66268361-66268655 | Common:3; Rare:87 | ||||
| chr11:66288954-66289393 | Common:2; Rare:114 | ||||
| chr11:66347550-66347879 | Common:5; Rare:81; Clinvar (benign):2 |