| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65712172-65712288 | Rare:43 | ||||
| chr11:65720431-65720599 | Common:1; Rare:87 | ||||
| chr11:65720758-65721061 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:65856996-65857325 | Common:4; Rare:99 | ||||
| chr11:65860166-65860459 | Common:1; Rare:95 | ||||
| chr11:65872687-65872951 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65888426-65888686 | Common:1; Rare:90 | ||||
| chr11:65890457-65890730 | Common:4; Rare:88 | ||||
| chr11:65900371-65900423 | Common:1; Rare:9 | ||||
| chr11:65961628-65961758 | Rare:42 | ||||
| chr11:66002097-66002266 | Rare:52; Clinvar:5 | ||||
| chr11:66002456-66002543 | Rare:24; Clinvar:1 | ||||
| chr11:66257618-66257828 | Rare:61 | ||||
| chr11:66268340-66268676 | Common:3; Rare:96 | ||||
| chr11:66289072-66289398 | Common:1; Rare:77 |