| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65712215-65712288 | Rare:24 | ||||
| chr11:65720482-65720578 | Common:1; Rare:54 | ||||
| chr11:65859320-65859624 | Rare:87 | ||||
| chr11:65860366-65860452 | Common:1; Rare:27 | ||||
| chr11:65873565-65873748 | Common:2; Rare:64 | ||||
| chr11:65888426-65888576 | Common:1; Rare:59 | ||||
| chr11:65920932-65921135 | Common:1; Rare:53 | ||||
| chr11:65961541-65961748 | Rare:70 | ||||
| chr11:66002108-66002561 | Common:3; Rare:129; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:66257613-66257832 | Rare:65 | ||||
| chr11:66268404-66268655 | Common:3; Rare:72 | ||||
| chr11:66288999-66289393 | Common:1; Rare:97 | ||||
| chr11:66345030-66345203 | Common:1; Rare:49 | ||||
| chr11:66347550-66347869 | Common:5; Rare:79; Clinvar (benign):2 | ||||
| chr11:66438766-66439133 | Common:1; Rare:92 |