Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44164941-44165133 | Common:1; Rare:45 | ||||
chr19:44212402-44212575 | Rare:43 | ||||
chr19:45370555-45370799 | Common:2; Rare:72 | ||||
chr19:45406337-45406687 | Common:2; Rare:87 | ||||
chr19:45423509-45423779 | Common:2; Rare:53; Clinvar (benign):1 | ||||
chr19:45507223-45507508 | Common:1; Rare:75 | ||||
chr19:46346951-46347111 | Common:3; Rare:46 | ||||
chr19:46600913-46601118 | Common:2; Rare:86 | ||||
chr19:46601186-46601370 | Common:3; Rare:52 | ||||
chr19:46850206-46850381 | Rare:24 | ||||
chr19:47113097-47113429 | Common:2; Rare:88 | ||||
chr19:47256423-47256564 | Rare:44 | ||||
chr19:47349088-47349350 | Rare:73 | ||||
chr19:48170259-48170699 | Common:2; Rare:120 | ||||
chr19:48445881-48446033 | Common:1; Rare:57 |