Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7395036-7395176 | Common:4; Rare:44 | ||||
chr19:7535445-7535740 | Common:3; Rare:90; Clinvar:2 | ||||
chr19:7629523-7629859 | Common:5; Rare:119; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7636989-7637143 | Common:2; Rare:51; Clinvar (benign):1 | ||||
chr19:7910694-7911156 | Common:3; Rare:174 | ||||
chr19:7943629-7943988 | Rare:102 | ||||
chr19:8005530-8005821 | Common:1; Rare:102 | ||||
chr19:8321308-8321703 | Common:2; Rare:159 | ||||
chr19:8364014-8364162 | Common:1; Rare:38 | ||||
chr19:8390032-8390412 | Common:1; Rare:106 | ||||
chr19:8444791-8445079 | Common:4; Rare:130; Clinvar (benign):1 | ||||
chr19:9140319-9140456 | Common:1; Rare:42 | ||||
chr19:9538603-9538718 | Common:1; Rare:33 | ||||
chr19:9621184-9621505 | Common:3; Rare:91 | ||||
chr19:9768661-9768763 | Common:1; Rare:30 |