Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:65009736-65009746 | Rare:1 | ||||
chr1:65066720-65066952 | Rare:75 | ||||
chr1:65067690-65067887 | Rare:51 | ||||
chr1:65426228-65426473 | Rare:67 | ||||
chr1:66942418-66942670 | Rare:46 | ||||
chr1:66959441-66959711 | Common:1; Rare:64 | ||||
chr1:67831904-67832237 | Common:1; Rare:70 | ||||
chr1:68159140-68159323 | Common:1; Rare:53 | ||||
chr1:68159806-68160037 | Common:1; Rare:41 | ||||
chr1:68217375-68217649 | Rare:53 | ||||
chr1:70353964-70354110 | Rare:36 | ||||
chr1:74714582-74714898 | Common:5; Rare:71 | ||||
chr1:77128824-77129090 | Common:3; Rare:51 | ||||
chr1:77613088-77613198 | Rare:19 | ||||
chr1:77942256-77942529 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):1 |