Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35039230-35039333 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):3 | ||||
chr19:35551087-35551366 | Common:1; Rare:59 | ||||
chr19:36142725-36142961 | Rare:55 | ||||
chr19:36266571-36266689 | Common:5; Rare:64 | ||||
chr19:36309438-36309580 | Common:2; Rare:31 | ||||
chr19:36322003-36322286 | Common:4; Rare:64 | ||||
chr19:36331628-36331967 | Common:2; Rare:86 | ||||
chr19:36797313-36797564 | Common:1; Rare:51 | ||||
chr19:36797634-36797677 | Rare:5 | ||||
chr19:37251638-37251930 | Common:6; Rare:75 | ||||
chr19:37304338-37304455 | Common:2; Rare:72 | ||||
chr19:38683693-38683898 | Common:2; Rare:34 | ||||
chr19:38710218-38710306 | Rare:25; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:38845671-38845912 | Common:1; Rare:71 | ||||
chr19:39409655-39409800 | Rare:35 |