Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47349050-47349389 | Common:1; Rare:100 | ||||
chr19:47484153-47484304 | Common:2; Rare:52 | ||||
chr19:47607989-47608205 | Common:1; Rare:54 | ||||
chr19:47780498-47780747 | Common:1; Rare:65 | ||||
chr19:48170287-48170705 | Common:2; Rare:112 | ||||
chr19:48390881-48390970 | Rare:9 | ||||
chr19:48445886-48446077 | Common:1; Rare:77 | ||||
chr19:48469075-48469402 | Common:3; Rare:96 | ||||
chr19:48619139-48619479 | Common:1; Rare:113 | ||||
chr19:48624057-48624414 | Common:1; Rare:87 | ||||
chr19:48810993-48811124 | Rare:47 | ||||
chr19:48835818-48835970 | Common:1; Rare:48 | ||||
chr19:48965242-48965916 | Common:1; Rare:231; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
chr19:48993253-48993536 | Common:3; Rare:126; Clinvar:3; Clinvar (benign):2 | ||||
chr19:48993553-48993910 | Common:5; Rare:93 |