Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37317666-37317923 | Common:6; Rare:63 | ||||
chr19:37334530-37334710 | Rare:70 | ||||
chr19:37370917-37371213 | Common:5; Rare:64 | ||||
chr19:37467160-37467530 | Common:2; Rare:107 | ||||
chr19:37469181-37469405 | Common:2; Rare:65 | ||||
chr19:37551268-37551389 | Rare:43 | ||||
chr19:37594753-37594910 | Rare:44 | ||||
chr19:37779567-37779662 | Rare:22 | ||||
chr19:37817300-37817520 | Common:1; Rare:44 | ||||
chr19:38374920-38374949 | Common:1; Rare:4 | ||||
chr19:38618947-38619326 | Common:3; Rare:103 | ||||
chr19:38647372-38647713 | Common:3; Rare:120 | ||||
chr19:38815613-38816011 | Common:2; Rare:136; Clinvar (benign):1 | ||||
chr19:38831664-38832061 | Common:6; Rare:128; Clinvar (benign):1 | ||||
chr19:38852319-38852362 | Rare:12 |