Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44808932-44809136 | Rare:70 | ||||
chr19:44954911-44955017 | Common:2; Rare:31 | ||||
chr19:44955237-44955531 | Common:2; Rare:95 | ||||
chr19:45038943-45039105 | Rare:58 | ||||
chr19:45079171-45079322 | Rare:41 | ||||
chr19:45091485-45091804 | Common:2; Rare:90 | ||||
chr19:45092827-45093143 | Common:2; Rare:91 | ||||
chr19:45322924-45323289 | Common:2; Rare:80 | ||||
chr19:45370537-45370679 | Rare:49 | ||||
chr19:45405019-45405212 | Common:1; Rare:42 | ||||
chr19:45406290-45406670 | Common:1; Rare:86 | ||||
chr19:45496959-45497278 | Common:3; Rare:96 | ||||
chr19:45507386-45507673 | Rare:86 | ||||
chr19:45584757-45585093 | Common:4; Rare:122; Clinvar:2; Clinvar (benign):4 | ||||
chr19:45692374-45692722 | Common:1; Rare:84 |