Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40026744-40026890 | Common:8; Rare:33 | ||||
chr19:40582429-40582746 | Common:1; Rare:74 | ||||
chr19:40607246-40607530 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
chr19:40752170-40752393 | Common:1; Rare:53 | ||||
chr19:40765377-40765511 | Common:1; Rare:21 | ||||
chr19:40812116-40812443 | Common:5; Rare:58 | ||||
chr19:41089777-41089903 | Common:5; Rare:62 | ||||
chr19:41176205-41176338 | Common:1; Rare:23 | ||||
chr19:41189421-41189695 | Rare:45 | ||||
chr19:41192254-41192374 | Rare:23 | ||||
chr19:41194287-41194691 | Common:4; Rare:105 | ||||
chr19:41352937-41353124 | Common:4; Rare:63; Clinvar (benign):2 | ||||
chr19:41542752-41543053 | Common:1; Rare:52 | ||||
chr19:41615886-41616184 | Common:1; Rare:52 | ||||
chr19:41867419-41867471 | Common:1; Rare:7 |