Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26336400-26336840 | Common:3; Rare:183 | ||||
chr1:26410624-26410838 | Common:1; Rare:47 | ||||
chr1:26432085-26432414 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472244-26472452 | Common:4; Rare:59 | ||||
chr1:26472819-26473339 | Common:2; Rare:354 | ||||
chr1:26529605-26529786 | Common:2; Rare:61 | ||||
chr1:26695394-26695758 | Common:1; Rare:110 | ||||
chr1:26695926-26696103 | Rare:53 | ||||
chr1:26786938-26787126 | Rare:40 | ||||
chr1:26787841-26788257 | Common:3; Rare:125; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26826482-26826728 | Rare:70 | ||||
chr1:26890248-26890411 | Common:1; Rare:72 | ||||
chr1:26899980-26900290 | Rare:120 | ||||
chr1:26900425-26900583 | Rare:54 | ||||
chr1:26921495-26921803 | Common:3; Rare:87 |