Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:103585455-103585682 | Common:3; Rare:46 | ||||
chrX:103628898-103629019 | Rare:16 | ||||
chrX:103629445-103629527 | Rare:23 | ||||
chrX:103686980-103687288 | Rare:47 | ||||
chrX:103774153-103774453 | Common:7; Rare:38 | ||||
chrX:103776711-103776982 | Common:2; Rare:37; Clinvar (benign):1 | ||||
chrX:104156894-104157063 | Common:1; Rare:28 | ||||
chrX:107118775-107118899 | Common:2; Rare:27 | ||||
chrX:107628340-107628526 | Common:1; Rare:21; Clinvar (benign):1 | ||||
chrX:107715741-107716068 | Common:1; Rare:48 | ||||
chrX:107716069-107716849 | Common:1; Rare:134 | ||||
chrX:107716853-107716900 | Rare:4 | ||||
chrX:107716904-107717193 | Common:2; Rare:35 | ||||
chrX:107775610-107775907 | Rare:50 | ||||
chrX:108091516-108091818 | Rare:80 |