Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25859332-25859616 | Common:3; Rare:120 | ||||
chr1:25892569-25892708 | Common:3; Rare:25 | ||||
chr1:25998159-25998454 | Common:3; Rare:79 | ||||
chr1:26233873-26234276 | Common:4; Rare:122 | ||||
chr1:26234405-26234482 | Common:2; Rare:27 | ||||
chr1:26279917-26280158 | Rare:138 | ||||
chr1:26306603-26306833 | Common:7; Rare:56 | ||||
chr1:26432091-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472314-26472627 | Common:4; Rare:120 | ||||
chr1:26695722-26696047 | Common:1; Rare:105 | ||||
chr1:26787865-26788257 | Common:3; Rare:113; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26862974-26863171 | Rare:40 | ||||
chr1:26890205-26890377 | Common:1; Rare:66 | ||||
chr1:26900411-26900547 | Rare:50 | ||||
chr1:26921529-26921926 | Common:3; Rare:123 |