Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161159365-161159526 | Common:2; Rare:44 | ||||
chr1:161166268-161166512 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161197212-161197428 | Common:2; Rare:37 | ||||
chr1:161199051-161199285 | Rare:37 | ||||
chr1:161215172-161215310 | Common:2; Rare:47 | ||||
chr1:161225826-161226069 | Common:9; Rare:34 | ||||
chr1:161309955-161310251 | Common:1; Rare:44 | ||||
chr1:161314267-161314414 | Common:3; Rare:56; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367864-161367905 | Rare:10 | ||||
chr1:161524369-161524546 | Common:3; Rare:58 | ||||
chr1:161549794-161549898 | Rare:36 | ||||
chr1:161750274-161750460 | Rare:32 | ||||
chr1:161766157-161766376 | Common:3; Rare:67 | ||||
chr1:162023432-162023448 | Rare:7 | ||||
chr1:162023568-162023575 | Rare:2 |