| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65614175-65614344 | Rare:43 | ||||
| chr11:65642340-65642633 | Common:1; Rare:68 | ||||
| chr11:65662828-65663320 | Common:4; Rare:122 | ||||
| chr11:65711868-65712039 | Rare:52 | ||||
| chr11:65720457-65720565 | Common:1; Rare:62 | ||||
| chr11:65857005-65857325 | Common:4; Rare:95 | ||||
| chr11:65860165-65860754 | Common:3; Rare:189 | ||||
| chr11:65873557-65873808 | Common:3; Rare:80 | ||||
| chr11:65888392-65888682 | Common:1; Rare:102 | ||||
| chr11:65890451-65890752 | Common:4; Rare:96 | ||||
| chr11:65961628-65961773 | Rare:50 | ||||
| chr11:66002097-66002399 | Common:3; Rare:91; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:66002466-66002818 | Common:1; Rare:98; Clinvar:1 | ||||
| chr11:66257614-66257845 | Rare:68 | ||||
| chr11:66268394-66268682 | Common:3; Rare:87 |