Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38930739-38930987 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391077-39391419 | Common:1; Rare:141 | ||||
chr19:39406735-39406852 | Rare:49 | ||||
chr19:39846335-39846468 | Common:1; Rare:59 | ||||
chr19:39970935-39971200 | Common:4; Rare:75 | ||||
chr19:40056168-40056238 | Rare:12 | ||||
chr19:40348511-40348713 | Common:3; Rare:60 | ||||
chr19:40751064-40751220 | Common:1; Rare:40 | ||||
chr19:41219146-41219228 | Rare:12 | ||||
chr19:41262412-41262565 | Rare:27 | ||||
chr19:41397556-41397821 | Common:7; Rare:93; Clinvar (benign):4 | ||||
chr19:42132397-42132621 | Rare:48 | ||||
chr19:43619602-43619720 | Common:2; Rare:32 | ||||
chr19:45079188-45079290 | Rare:27 | ||||
chr19:45405050-45405163 | Rare:23 |