Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:100820208-100820419 | Common:2; Rare:46 | ||||
chrX:101407899-101408284 | Common:5; Rare:69; Clinvar (benign):9 | ||||
chrX:103585455-103585643 | Common:3; Rare:42 | ||||
chrX:103629445-103629520 | Rare:21 | ||||
chrX:104156923-104157069 | Common:1; Rare:28 | ||||
chrX:107716995-107717182 | Common:1; Rare:25 | ||||
chrX:107775751-107775895 | Rare:31 | ||||
chrX:108091513-108091818 | Rare:80 | ||||
chrX:108439489-108439838 | Common:2; Rare:82 | ||||
chrX:119574374-119574592 | Rare:48 | ||||
chrX:119791590-119791978 | Common:2; Rare:102 | ||||
chrX:119871666-119871903 | Common:1; Rare:53; Clinvar (benign):2 | ||||
chrX:120560346-120560858 | Rare:88; Clinvar:2 | ||||
chrX:120630023-120630356 | Common:4; Rare:72 | ||||
chrX:123733019-123733137 | Rare:20 |