Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39846335-39846539 | Common:1; Rare:96 | ||||
chr19:40348364-40348713 | Common:4; Rare:109 | ||||
chr19:40425982-40426147 | Common:1; Rare:48 | ||||
chr19:46601209-46601370 | Common:3; Rare:46 | ||||
chr19:48170266-48170676 | Common:2; Rare:114 | ||||
chr19:48619144-48619324 | Rare:69 | ||||
chr19:48965273-48965916 | Common:1; Rare:226; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
chr19:48993290-48993533 | Common:3; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
chr19:49487335-49487644 | Common:5; Rare:113 | ||||
chr19:49665761-49666038 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
chr19:50384326-50384380 | Rare:21; Clinvar:1; Clinvar (benign):2 | ||||
chr19:50476422-50476542 | Rare:49 | ||||
chr19:51366335-51366595 | Common:8; Rare:73; Clinvar (benign):2 | ||||
chr19:52397750-52397878 | Common:2; Rare:37 | ||||
chr19:54102673-54102875 | Common:3; Rare:53 |