Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1605413-1605673 | Common:3; Rare:102 | ||||
chr19:2328559-2328691 | Rare:63 | ||||
chr19:5622768-5623139 | Common:5; Rare:130 | ||||
chr19:7629520-7629838 | Common:5; Rare:114; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:8321346-8321537 | Common:2; Rare:83 | ||||
chr19:9621192-9621493 | Common:3; Rare:86 | ||||
chr19:9835042-9835340 | Rare:123 | ||||
chr19:12551452-12551676 | Common:2; Rare:59 | ||||
chr19:14529284-14529627 | Common:1; Rare:141 | ||||
chr19:18919339-18919678 | Common:1; Rare:107 | ||||
chr19:19192124-19192212 | Common:1; Rare:30 | ||||
chr19:34677570-34677729 | Common:4; Rare:45 | ||||
chr19:35545340-35545689 | Common:4; Rare:105 | ||||
chr19:35745406-35745657 | Rare:79 | ||||
chr19:36215078-36215171 | Rare:31 |