Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65494515-65494797 | Rare:58 | ||||
chr11:65497440-65497843 | Common:1; Rare:178 | ||||
chr11:65504194-65505107 | Common:3; Rare:433 | ||||
chr11:65506665-65506909 | Common:4; Rare:79 | ||||
chr11:65526000-65526276 | Rare:94; Clinvar (pathogenic):1 | ||||
chr11:65899321-65899524 | Rare:41 | ||||
chr11:65912901-65913133 | Rare:45 | ||||
chr11:65914531-65914717 | Common:3; Rare:36 | ||||
chr11:65915753-65915982 | Rare:52 | ||||
chr11:65965808-65965977 | Common:2; Rare:50 | ||||
chr11:66315078-66315215 | Rare:32 | ||||
chr11:66315836-66315938 | Common:1; Rare:28 | ||||
chr11:66879552-66879824 | Common:2; Rare:36 | ||||
chr11:67277047-67277324 | Rare:67 | ||||
chr11:67438912-67439189 | Rare:72 |