Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44164921-44165136 | Common:1; Rare:51 | ||||
chr19:44304992-44305131 | Rare:38 | ||||
chr19:44643801-44643932 | Rare:36 | ||||
chr19:45322819-45323212 | Common:2; Rare:87 | ||||
chr19:45406340-45406694 | Common:3; Rare:89 | ||||
chr19:45863108-45863359 | Common:4; Rare:86 | ||||
chr19:46495865-46495876 | Rare:1 | ||||
chr19:46600913-46601100 | Common:2; Rare:75 | ||||
chr19:46601200-46601416 | Common:3; Rare:65; Clinvar (benign):1 | ||||
chr19:46746017-46746066 | Common:3; Rare:15 | ||||
chr19:47256459-47256568 | Rare:40 | ||||
chr19:47484042-47484318 | Common:2; Rare:93; Clinvar:1 | ||||
chr19:47608189-47608205 | Rare:3 | ||||
chr19:47780671-47780915 | Common:5; Rare:91 | ||||
chr19:48170324-48170704 | Common:2; Rare:94 |