Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48445768-48446140 | Common:2; Rare:139 | ||||
chr19:48619139-48619560 | Common:1; Rare:138 | ||||
chr19:48836452-48836585 | Rare:20 | ||||
chr19:48955164-48955340 | Common:1; Rare:41 | ||||
chr19:48955408-48955723 | Common:2; Rare:86; Clinvar (pathogenic):1 | ||||
chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr19:48993253-48993914 | Common:8; Rare:229; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49085103-49085521 | Common:3; Rare:168 | ||||
chr19:49362367-49362503 | Rare:39 | ||||
chr19:49453024-49453315 | Common:2; Rare:89 | ||||
chr19:49527864-49528031 | Common:3; Rare:51 | ||||
chr19:49580528-49580654 | Rare:42 | ||||
chr19:49665709-49666041 | Common:3; Rare:151; Clinvar (pathogenic):1 | ||||
chr19:49690980-49691144 | Common:1; Rare:37 | ||||
chr19:49813267-49813350 | Rare:37 |