Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6416824-6417072 | Common:1; Rare:85 | ||||
chr19:7533901-7534191 | Common:3; Rare:68; Clinvar (benign):1 | ||||
chr19:7535631-7535795 | Common:2; Rare:58 | ||||
chr19:7629530-7629842 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7636989-7637149 | Common:2; Rare:51; Clinvar (benign):1 | ||||
chr19:7920184-7920390 | Rare:82 | ||||
chr19:8308302-8308638 | Common:2; Rare:107 | ||||
chr19:8321324-8321497 | Common:2; Rare:77 | ||||
chr19:8390018-8390441 | Common:2; Rare:118 | ||||
chr19:8444903-8445109 | Rare:91; Clinvar (benign):1 | ||||
chr19:8514121-8514280 | Common:2; Rare:49 | ||||
chr19:9538574-9538739 | Common:1; Rare:52 | ||||
chr19:9621162-9621583 | Common:4; Rare:128 | ||||
chr19:9827833-9827954 | Common:1; Rare:47 | ||||
chr19:10251771-10251989 | Common:1; Rare:51 |