Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21831203-21831724 | Common:3; Rare:158; Clinvar:5; Clinvar (benign):2 | ||||
chr1:21833469-21833953 | Common:6; Rare:124; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:21878431-21878654 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):1 | ||||
chr1:21895919-21896313 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
chr1:21937180-21937665 | Common:10; Rare:125 | ||||
chr1:21937678-21937748 | Rare:13 | ||||
chr1:22052520-22052780 | Common:3; Rare:90 | ||||
chr1:22451644-22452011 | Common:2; Rare:90 | ||||
chr1:23019271-23019602 | Rare:114 | ||||
chr1:23019794-23019948 | Rare:38; Clinvar:1 | ||||
chr1:23019968-23020204 | Common:1; Rare:66 | ||||
chr1:23076992-23077348 | Common:1; Rare:71 | ||||
chr1:23080467-23080697 | Common:2; Rare:49 | ||||
chr1:23080698-23081053 | Common:3; Rare:77 | ||||
chr1:23168223-23168362 | Rare:19 |