Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36797291-36797546 | Rare:55 | ||||
chr19:46133324-46133607 | Rare:49 | ||||
chr19:46860822-46861121 | Common:3; Rare:98 | ||||
chr19:48873041-48873321 | Common:2; Rare:55 | ||||
chr19:48966350-48966649 | Rare:88; Clinvar:1 | ||||
chr19:49491525-49491736 | Common:1; Rare:70 | ||||
chr19:50896663-50896854 | Common:3; Rare:36 | ||||
chr19:52923414-52923532 | Common:2; Rare:46 | ||||
chr19:52942524-52942731 | Common:6; Rare:73 | ||||
chr19:52993507-52993783 | Common:3; Rare:57 | ||||
chr2:5696008-5696041 | Rare:5 | ||||
chr2:5981585-5981929 | Common:1; Rare:68 | ||||
chr2:20447769-20447807 | Rare:10 | ||||
chr2:26273586-26273741 | Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
chr2:47906488-47906815 | Common:2; Rare:114 |