Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10928397-10928897 | Common:3; Rare:156 | ||||
chr19:11089307-11089503 | Rare:28; Clinvar:8; Clinvar (pathogenic):1 | ||||
chr19:11155776-11156077 | Common:3; Rare:73 | ||||
chr19:11197489-11197676 | Common:1; Rare:58 | ||||
chr19:11559206-11559407 | Common:1; Rare:61 | ||||
chr19:12610811-12610963 | Rare:57 | ||||
chr19:12666693-12666830 | Rare:55; Clinvar:4 | ||||
chr19:12791281-12791494 | Rare:47 | ||||
chr19:12956974-12957065 | Common:2; Rare:43 | ||||
chr19:13023495-13023597 | Rare:23 | ||||
chr19:13023744-13023994 | Rare:48 | ||||
chr19:13150212-13150499 | Common:2; Rare:93 | ||||
chr19:13906096-13906302 | Rare:48 | ||||
chr19:13953371-13953518 | Rare:32 | ||||
chr19:14529255-14529659 | Common:1; Rare:163 |