Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40609517-40609854 | Common:1; Rare:111; Clinvar (benign):5 | ||||
chr19:40611922-40612192 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):6 | ||||
chr19:40623472-40623753 | Rare:80; Clinvar:1 | ||||
chr19:40715074-40715167 | Rare:27 | ||||
chr19:40716872-40717015 | Common:1; Rare:49 | ||||
chr19:40798911-40799242 | Common:6; Rare:122 | ||||
chr19:41218668-41218989 | Common:8; Rare:71 | ||||
chr19:41219147-41219449 | Common:1; Rare:80 | ||||
chr19:41220515-41220756 | Common:1; Rare:76 | ||||
chr19:41264061-41264510 | Common:3; Rare:145 | ||||
chr19:42069303-42069464 | Rare:30 | ||||
chr19:42070199-42070259 | Rare:11 | ||||
chr19:42075785-42076191 | Common:4; Rare:114 | ||||
chr19:42132420-42132621 | Rare:40 | ||||
chr19:42412394-42412445 | Rare:9 |