| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65856951-65857319 | Common:4; Rare:112 | ||||
| chr11:65860143-65860754 | Common:4; Rare:195 | ||||
| chr11:65867036-65867110 | Rare:27; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:65872722-65872960 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65873550-65873691 | Common:2; Rare:45 | ||||
| chr11:65879788-65879842 | Common:1; Rare:17 | ||||
| chr11:65888358-65888686 | Common:1; Rare:107 | ||||
| chr11:65890436-65890730 | Common:5; Rare:92 | ||||
| chr11:65900382-65900492 | Common:1; Rare:19 | ||||
| chr11:65920344-65920647 | Rare:103 | ||||
| chr11:65961476-65961783 | Common:1; Rare:105 | ||||
| chr11:65977607-65977896 | Common:1; Rare:93 | ||||
| chr11:66002102-66002369 | Common:3; Rare:81; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:66002456-66002543 | Rare:24; Clinvar:1 | ||||
| chr11:66058054-66058786 | Common:4; Rare:163 |