Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44500505-44500653 | Common:3; Rare:40 | ||||
chr19:44643793-44643918 | Rare:39 | ||||
chr19:44757401-44757576 | Rare:39 | ||||
chr19:45091583-45091752 | Common:1; Rare:45 | ||||
chr19:45406321-45406649 | Common:1; Rare:68 | ||||
chr19:45423466-45423821 | Common:3; Rare:72; Clinvar (benign):1 | ||||
chr19:45450743-45450999 | Common:4; Rare:47 | ||||
chr19:45468293-45468462 | Rare:40 | ||||
chr19:45468493-45468601 | Rare:16 | ||||
chr19:45469143-45469500 | Common:2; Rare:115 | ||||
chr19:45478685-45478815 | Common:2; Rare:74 | ||||
chr19:45507228-45507523 | Common:1; Rare:79 | ||||
chr19:45768251-45768293 | Rare:16 | ||||
chr19:45769207-45769363 | Rare:53 | ||||
chr19:45863125-45863334 | Common:3; Rare:65 |