Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:43935242-43935325 | Common:2; Rare:23 | ||||
chr19:44071952-44072181 | Common:1; Rare:54 | ||||
chr19:44113175-44113440 | Common:3; Rare:58 | ||||
chr19:44141472-44141643 | Common:2; Rare:23 | ||||
chr19:44164955-44165133 | Common:1; Rare:41 | ||||
chr19:44212437-44212575 | Rare:36 | ||||
chr19:44500205-44500263 | Common:1; Rare:29 | ||||
chr19:44643793-44644047 | Common:1; Rare:67 | ||||
chr19:44808972-44809121 | Rare:56 | ||||
chr19:45038951-45039104 | Rare:54 | ||||
chr19:45079130-45079311 | Common:1; Rare:47 | ||||
chr19:45370548-45370782 | Common:2; Rare:71 | ||||
chr19:45406355-45406695 | Common:3; Rare:87 | ||||
chr19:45423477-45423790 | Common:2; Rare:65; Clinvar (benign):1 | ||||
chr19:45423839-45423992 | Common:2; Rare:34 |