Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:126776931-126777187 | Common:1; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
chr5:127073471-127073563 | Common:3; Rare:28 | ||||
chr5:129094490-129094759 | Common:3; Rare:110 | ||||
chr5:131170701-131170984 | Common:1; Rare:56 | ||||
chr5:131635215-131635353 | Common:1; Rare:51 | ||||
chr5:132073652-132073819 | Rare:25 | ||||
chr5:132866334-132866683 | Common:1; Rare:106; Clinvar (benign):1 | ||||
chr5:133051870-133052091 | Rare:82 | ||||
chr5:133968570-133968737 | Rare:65 | ||||
chr5:134004654-134004877 | Common:1; Rare:85 | ||||
chr5:134004941-134005111 | Rare:37 | ||||
chr5:134411846-134412111 | Common:1; Rare:77 | ||||
chr5:134648711-134648816 | Rare:26 | ||||
chr5:134738335-134738570 | Rare:83 | ||||
chr5:135399119-135399346 | Rare:60 |