Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:13507423-13507585 | Common:2; Rare:34 | ||||
chr19:14565949-14566083 | Common:1; Rare:55 | ||||
chr19:15223356-15223643 | Common:3; Rare:62 | ||||
chr19:18279696-18279795 | Rare:41 | ||||
chr19:18280063-18280249 | Common:1; Rare:65 | ||||
chr19:18428947-18429084 | Common:1; Rare:38 | ||||
chr19:18879138-18879363 | Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
chr19:18894231-18894420 | Rare:50 | ||||
chr19:19032497-19032705 | Common:3; Rare:33 | ||||
chr19:19489294-19489527 | Rare:37 | ||||
chr19:19776363-19776632 | Common:3; Rare:76 | ||||
chr19:20238371-20238569 | Common:1; Rare:58 | ||||
chr19:20999714-20999951 | Common:3; Rare:56 | ||||
chr19:21463835-21464023 | Common:1; Rare:46 | ||||
chr19:23273940-23274005 | Common:1; Rare:15 |