Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38723630-38723994 | Common:1; Rare:96; Clinvar (benign):1 | ||||
chr19:38831762-38831963 | Common:4; Rare:70; Clinvar (benign):1 | ||||
chr19:38842209-38842343 | Rare:25 | ||||
chr19:38842449-38842469 | Rare:4 | ||||
chr19:38899561-38900033 | Rare:143 | ||||
chr19:38930738-38931002 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39390990-39391439 | Common:1; Rare:173 | ||||
chr19:39834124-39834476 | Common:3; Rare:93 | ||||
chr19:39846341-39846470 | Common:1; Rare:56 | ||||
chr19:39996969-39997118 | Common:4; Rare:50 | ||||
chr19:40056163-40056275 | Rare:18 | ||||
chr19:40348381-40348746 | Common:4; Rare:122 | ||||
chr19:40715068-40715173 | Rare:31 | ||||
chr19:40716879-40717129 | Common:1; Rare:76 | ||||
chr19:40750433-40750622 | Common:5; Rare:58 |