Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65317386-65317667 | Common:2; Rare:41 | ||||
chr11:65333745-65333901 | Common:1; Rare:77 | ||||
chr11:65382367-65382781 | Common:3; Rare:81 | ||||
chr11:65503607-65504134 | Common:1; Rare:265 | ||||
chr11:65535790-65535926 | Rare:25 | ||||
chr11:65536278-65536548 | Rare:57; Clinvar (pathogenic):1 | ||||
chr11:65557639-65557849 | Rare:54; Clinvar (pathogenic):1 | ||||
chr11:65570356-65570510 | Rare:66 | ||||
chr11:65614176-65614423 | Rare:55 | ||||
chr11:65615234-65615318 | Rare:21 | ||||
chr11:65616023-65616211 | Rare:58 | ||||
chr11:65662664-65663019 | Common:1; Rare:89 | ||||
chr11:65711826-65712060 | Rare:75 | ||||
chr11:65720457-65720694 | Common:1; Rare:117; Clinvar:1 | ||||
chr11:65856948-65857329 | Common:4; Rare:113 |