| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65860356-65860459 | Common:1; Rare:31 | ||||
| chr11:65888402-65888637 | Common:1; Rare:86 | ||||
| chr11:65920158-65920462 | Common:1; Rare:90 | ||||
| chr11:65961517-65961769 | Common:1; Rare:88 | ||||
| chr11:66002087-66002266 | Rare:55; Clinvar:6 | ||||
| chr11:66002458-66002847 | Common:1; Rare:109; Clinvar:1 | ||||
| chr11:66049120-66049339 | Common:2; Rare:38 | ||||
| chr11:66257559-66257864 | Common:1; Rare:89 | ||||
| chr11:66268404-66268655 | Common:3; Rare:72 | ||||
| chr11:66278448-66278535 | Rare:19 | ||||
| chr11:66288992-66289418 | Common:1; Rare:109 | ||||
| chr11:66291689-66291894 | Common:1; Rare:51 | ||||
| chr11:66345036-66345203 | Common:1; Rare:49 | ||||
| chr11:66347496-66347890 | Common:5; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:66438758-66439172 | Common:2; Rare:102 |