Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45406308-45406738 | Common:3; Rare:106 | ||||
chr19:45423477-45423655 | Common:1; Rare:37; Clinvar (benign):1 | ||||
chr19:45423851-45423942 | Common:2; Rare:25 | ||||
chr19:45496957-45497281 | Common:3; Rare:97 | ||||
chr19:45499408-45499800 | Common:2; Rare:123 | ||||
chr19:45506851-45506969 | Rare:34 | ||||
chr19:45507414-45507566 | Rare:50 | ||||
chr19:45615872-45615948 | Rare:27 | ||||
chr19:45615984-45616331 | Common:1; Rare:86 | ||||
chr19:45639220-45639482 | Common:1; Rare:68 | ||||
chr19:45677396-45677661 | Common:2; Rare:50 | ||||
chr19:45692319-45692722 | Common:1; Rare:95 | ||||
chr19:45768226-45768425 | Rare:91; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:45768833-45768860 | Rare:8 | ||||
chr19:45769186-45769310 | Rare:31 |