Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39411515-39411710 | Common:2; Rare:38 | ||||
chr19:40245937-40246199 | Common:2; Rare:24 | ||||
chr19:40605290-40605571 | Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
chr19:40664011-40664212 | Rare:42 | ||||
chr19:40720610-40720888 | Common:2; Rare:52 | ||||
chr19:40810774-40810889 | Common:1; Rare:26 | ||||
chr19:41263679-41263757 | Rare:18 | ||||
chr19:41352787-41352801 | Rare:4 | ||||
chr19:41447812-41448106 | Common:1; Rare:47 | ||||
chr19:41500583-41500740 | Rare:26 | ||||
chr19:41531561-41531743 | Common:1; Rare:38 | ||||
chr19:42270464-42270558 | Rare:13 | ||||
chr19:42396905-42397188 | Common:1; Rare:66 | ||||
chr19:42419437-42419639 | Common:1; Rare:29 | ||||
chr19:42421629-42422125 | Rare:79 |