Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161098281-161098427 | Common:1; Rare:25 | ||||
chr1:161117982-161118382 | Common:1; Rare:166 | ||||
chr1:161132356-161132700 | Common:1; Rare:108 | ||||
chr1:161153720-161153836 | Rare:29 | ||||
chr1:161166268-161166512 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161197322-161197415 | Common:2; Rare:13 | ||||
chr1:161199038-161199326 | Rare:44 | ||||
chr1:161209340-161209577 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:161215109-161215366 | Common:2; Rare:82 | ||||
chr1:161314262-161314425 | Common:3; Rare:65; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161505282-161505542 | Common:1; Rare:55 | ||||
chr1:161524182-161524313 | Common:1; Rare:29 | ||||
chr1:161549772-161549898 | Rare:46 | ||||
chr1:161550529-161550671 | Common:2; Rare:26 | ||||
chr1:161749749-161749913 | Rare:65 |