Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26317813-26317968 | Common:2; Rare:21 | ||||
chr1:26336364-26336574 | Common:2; Rare:85 | ||||
chr1:26410607-26411108 | Common:1; Rare:120 | ||||
chr1:26411304-26411418 | Rare:29 | ||||
chr1:26432044-26432418 | Common:5; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472273-26472626 | Common:4; Rare:128 | ||||
chr1:26695580-26695785 | Rare:69 | ||||
chr1:26695933-26696048 | Rare:38 | ||||
chr1:26787819-26788250 | Common:3; Rare:128; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890229-26890428 | Common:1; Rare:91 | ||||
chr1:26900044-26900184 | Rare:50 | ||||
chr1:26900374-26900547 | Rare:77 | ||||
chr1:26921554-26921932 | Common:3; Rare:115 | ||||
chr1:26960357-26960528 | Common:1; Rare:35 | ||||
chr1:26993596-26993716 | Common:2; Rare:43 |