Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65575523-65576141 | Common:4; Rare:132 | ||||
chr11:65614038-65614553 | Rare:119 | ||||
chr11:65615038-65615189 | Common:1; Rare:23 | ||||
chr11:65615234-65615671 | Common:1; Rare:154 | ||||
chr11:65615712-65615910 | Common:1; Rare:56 | ||||
chr11:65616017-65616213 | Rare:61 | ||||
chr11:65637989-65638223 | Common:3; Rare:92 | ||||
chr11:65639628-65639932 | Rare:55 | ||||
chr11:65662873-65663371 | Common:4; Rare:124 | ||||
chr11:65711813-65712102 | Rare:88 | ||||
chr11:65712156-65712360 | Rare:85 | ||||
chr11:65712526-65712631 | Common:2; Rare:41 | ||||
chr11:65720447-65720627 | Common:1; Rare:91 | ||||
chr11:65720700-65720886 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr11:65780846-65781074 | Common:1; Rare:84 |