Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65444017-65444732 | Common:9; Rare:151 | ||||
chr11:65444971-65445205 | Common:1; Rare:42 | ||||
chr11:65455120-65455269 | Rare:68 | ||||
chr11:65497435-65497837 | Common:1; Rare:175 | ||||
chr11:65505495-65505905 | Rare:192 | ||||
chr11:65636494-65636833 | Common:5; Rare:109 | ||||
chr11:65890657-65890670 | Rare:7 | ||||
chr11:66718688-66718969 | Common:1; Rare:77 | ||||
chr11:66822353-66822637 | Common:2; Rare:53; Clinvar (pathogenic):1 | ||||
chr11:66905984-66906226 | Common:2; Rare:42 | ||||
chr11:67805300-67805611 | Common:3; Rare:115 | ||||
chr11:72004776-72004843 | Rare:16 | ||||
chr11:76963470-76963815 | Common:2; Rare:55 | ||||
chr11:78223657-78223810 | Rare:37 | ||||
chr11:79419290-79419343 | Rare:6 |