Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6065927-6066089 | Rare:21 | ||||
chr19:6103596-6103638 | Rare:8 | ||||
chr19:6108541-6108763 | Common:2; Rare:43 | ||||
chr19:6744424-6744646 | Common:1; Rare:71 | ||||
chr19:6766241-6766301 | Common:2; Rare:5 | ||||
chr19:7561341-7561605 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7615323-7615439 | Rare:43 | ||||
chr19:7622613-7622819 | Common:3; Rare:71 | ||||
chr19:7623168-7623459 | Rare:87 | ||||
chr19:8386697-8386799 | Common:3; Rare:25 | ||||
chr19:9656624-9656841 | Rare:59 | ||||
chr19:10005573-10005822 | Common:1; Rare:83 | ||||
chr19:10115735-10115904 | Common:2; Rare:68 | ||||
chr19:10561001-10561261 | Common:3; Rare:91 | ||||
chr19:11047847-11048128 | Common:1; Rare:78 |