Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2247135-2247355 | Common:2; Rare:49 | ||||
chr19:2392920-2393164 | Common:2; Rare:80 | ||||
chr19:2578103-2578239 | Common:1; Rare:28 | ||||
chr19:2763251-2763378 | Common:1; Rare:28 | ||||
chr19:2800812-2800915 | Common:1; Rare:48 | ||||
chr19:2926784-2926963 | Common:5; Rare:61 | ||||
chr19:3306864-3306997 | Rare:35 | ||||
chr19:3361178-3361223 | Rare:9 | ||||
chr19:3642918-3643217 | Common:4; Rare:129 | ||||
chr19:3977213-3977596 | Common:4; Rare:125; Clinvar (benign):8 | ||||
chr19:3990313-3990418 | Common:2; Rare:24 | ||||
chr19:4037122-4037398 | Common:2; Rare:108 | ||||
chr19:4471631-4471767 | Rare:33 | ||||
chr19:4640859-4640975 | Common:1; Rare:21 | ||||
chr19:4768951-4769146 | Rare:45 |