Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65614216-65614407 | Rare:36 | ||||
chr11:65662896-65663078 | Common:1; Rare:46 | ||||
chr11:65888415-65888676 | Common:1; Rare:91 | ||||
chr11:66002128-66002532 | Common:3; Rare:110; Clinvar:3; Clinvar (benign):3 | ||||
chr11:66289072-66289398 | Common:1; Rare:77 | ||||
chr11:66480239-66480444 | Common:1; Rare:54 | ||||
chr11:66593053-66593209 | Common:1; Rare:54 | ||||
chr11:66616398-66616646 | Common:1; Rare:67 | ||||
chr11:66677851-66678054 | Rare:74 | ||||
chr11:67401789-67402075 | Common:3; Rare:103 | ||||
chr11:68030317-68030744 | Common:3; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68271889-68272023 | Rare:65 | ||||
chr11:68903800-68903919 | Common:3; Rare:49; Clinvar (benign):2 | ||||
chr11:69640952-69641218 | Rare:58 | ||||
chr11:69675309-69675478 | Rare:47 |