Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10836277-10836571 | Common:2; Rare:77 | ||||
chr19:10928557-10928802 | Common:2; Rare:69 | ||||
chr19:10960650-10961167 | Common:6; Rare:199; Clinvar (benign):2 | ||||
chr19:11089281-11089516 | Rare:39; Clinvar:9; Clinvar (pathogenic):1 | ||||
chr19:11090334-11090604 | Common:2; Rare:79 | ||||
chr19:11155783-11156061 | Common:3; Rare:63 | ||||
chr19:11197520-11197676 | Common:1; Rare:52 | ||||
chr19:11339476-11339764 | Common:3; Rare:63 | ||||
chr19:11355231-11355534 | Common:1; Rare:90 | ||||
chr19:11355546-11355741 | Rare:32 | ||||
chr19:11374497-11374753 | Common:1; Rare:87 | ||||
chr19:11374865-11375233 | Common:2; Rare:116 | ||||
chr19:11435089-11435440 | Common:2; Rare:90 | ||||
chr19:11435503-11435677 | Common:3; Rare:57; Clinvar:1; Clinvar (benign):3 | ||||
chr19:11480610-11480687 | Rare:20 |