Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40720637-40720872 | Common:2; Rare:40 | ||||
chr19:40810790-40810836 | Rare:8 | ||||
chr19:41352929-41352992 | Common:1; Rare:22; Clinvar (benign):1 | ||||
chr19:42287188-42287447 | Common:1; Rare:85; Clinvar:2 | ||||
chr19:42292825-42293048 | Rare:75; Clinvar:3 | ||||
chr19:42396902-42397188 | Common:1; Rare:67 | ||||
chr19:44847594-44847653 | Rare:12 | ||||
chr19:45509355-45509518 | Common:1; Rare:45 | ||||
chr19:45717253-45717554 | Common:1; Rare:94 | ||||
chr19:46860910-46861133 | Common:1; Rare:76 | ||||
chr19:48966277-48966730 | Common:1; Rare:153; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:49491460-49491985 | Common:3; Rare:152 | ||||
chr19:52923406-52923535 | Common:3; Rare:53 | ||||
chr19:55240985-55241251 | Common:1; Rare:91 | ||||
chr19:58088749-58089019 | Rare:60 |