Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:160399196-160399307 | Rare:30; Clinvar:1 | ||||
chr3:160399532-160399721 | Rare:50 | ||||
chr3:160449715-160450038 | Common:2; Rare:111 | ||||
chr3:160565517-160565784 | Common:2; Rare:102 | ||||
chr3:161105075-161105354 | Common:3; Rare:81 | ||||
chr3:161221178-161221326 | Rare:46 | ||||
chr3:167734820-167735187 | Common:2; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
chr3:169773333-169773418 | Rare:24 | ||||
chr3:169812902-169813071 | Common:2; Rare:31 | ||||
chr3:169966734-169966844 | Rare:48 | ||||
chr3:170222360-170222539 | Common:1; Rare:62 | ||||
chr3:170870157-170870304 | Rare:80 | ||||
chr3:171460372-171460532 | Rare:35 | ||||
chr3:172039482-172039659 | Common:1; Rare:58 | ||||
chr3:172711011-172711103 | Rare:55 |