Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:16185168-16185448 | Common:1; Rare:89 | ||||
chr19:16197736-16198020 | Common:3; Rare:106 | ||||
chr19:16496172-16496424 | Common:2; Rare:60 | ||||
chr19:16542402-16542607 | Common:2; Rare:57 | ||||
chr19:17215282-17215423 | Common:2; Rare:58 | ||||
chr19:17511449-17511670 | Common:3; Rare:92 | ||||
chr19:17859600-17859969 | Common:2; Rare:111 | ||||
chr19:18323027-18323321 | Common:3; Rare:95 | ||||
chr19:18919344-18919783 | Common:3; Rare:165 | ||||
chr19:19033461-19033610 | Common:2; Rare:57 | ||||
chr19:19192115-19192268 | Common:1; Rare:50 | ||||
chr19:19192589-19192990 | Common:2; Rare:103 | ||||
chr19:19320476-19320854 | Common:4; Rare:138 | ||||
chr19:19516157-19516270 | Rare:66; Clinvar (pathogenic):1 | ||||
chr19:19668511-19668788 | Rare:65 |