Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39846289-39846473 | Common:1; Rare:84 | ||||
chr19:39970954-39971223 | Common:3; Rare:74 | ||||
chr19:39996956-39997113 | Common:4; Rare:55 | ||||
chr19:40056145-40056251 | Rare:15 | ||||
chr19:40090886-40090986 | Common:1; Rare:28 | ||||
chr19:40285243-40285562 | Common:1; Rare:116 | ||||
chr19:40348352-40348739 | Common:4; Rare:126 | ||||
chr19:40377835-40378070 | Common:2; Rare:91; Clinvar (benign):1 | ||||
chr19:40413356-40413543 | Rare:54 | ||||
chr19:40425975-40426166 | Common:1; Rare:60 | ||||
chr19:40465615-40466112 | Common:3; Rare:171 | ||||
chr19:40601214-40601384 | Rare:54 | ||||
chr19:40609535-40609803 | Common:1; Rare:83; Clinvar (benign):4 | ||||
chr19:40715068-40715171 | Rare:31 | ||||
chr19:40716867-40717011 | Common:1; Rare:50 |