Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47484261-47484300 | Rare:11 | ||||
chr19:48170324-48170664 | Common:2; Rare:88 | ||||
chr19:48619139-48619428 | Rare:92 | ||||
chr19:48965398-48965609 | Rare:65; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:48993296-48993510 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49114124-49114402 | Common:4; Rare:68 | ||||
chr19:49580543-49580645 | Rare:36 | ||||
chr19:49665765-49665980 | Common:2; Rare:102; Clinvar (pathogenic):1 | ||||
chr19:49877333-49877717 | Common:1; Rare:95 | ||||
chr19:49877839-49878156 | Common:4; Rare:98 | ||||
chr19:50476214-50476542 | Common:1; Rare:153 | ||||
chr19:51366339-51366551 | Common:5; Rare:55; Clinvar (benign):2 | ||||
chr19:51751866-51751987 | Common:2; Rare:26 | ||||
chr19:52008182-52008349 | Rare:46 | ||||
chr19:52397750-52397879 | Common:2; Rare:38 |