Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40777934-40778280 | Common:1; Rare:97 | ||||
chr19:41218636-41218966 | Common:7; Rare:71 | ||||
chr19:41262383-41262566 | Rare:32 | ||||
chr19:41310142-41310270 | Rare:53 | ||||
chr19:41363795-41363977 | Common:1; Rare:66; Clinvar:1 | ||||
chr19:41397321-41397606 | Common:4; Rare:75 | ||||
chr19:41860107-41860281 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
chr19:42075816-42076186 | Rare:101 | ||||
chr19:42220132-42220349 | Common:2; Rare:61 | ||||
chr19:42302435-42302498 | Rare:13 | ||||
chr19:43527151-43527303 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr19:43596312-43596644 | Rare:106 | ||||
chr19:43670127-43670309 | Common:2; Rare:43 | ||||
chr19:43754840-43755091 | Common:3; Rare:99 | ||||
chr19:43901762-43901892 | Common:3; Rare:27 |