Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:77895417-77895741 | Rare:89; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chrX:78103950-78104266 | Common:3; Rare:100 | ||||
chrX:81201893-81202168 | Rare:45 | ||||
chrX:101407897-101408275 | Common:5; Rare:69; Clinvar (benign):9 | ||||
chrX:103629468-103629505 | Rare:7 | ||||
chrX:104156978-104157069 | Rare:15 | ||||
chrX:106802439-106802731 | Common:1; Rare:56 | ||||
chrX:108091516-108091818 | Rare:80 | ||||
chrX:108439457-108439878 | Common:2; Rare:96 | ||||
chrX:110318077-110318273 | Rare:47 | ||||
chrX:119791601-119791716 | Rare:46 | ||||
chrX:119871673-119871905 | Common:1; Rare:55; Clinvar (benign):2 | ||||
chrX:120603796-120604143 | Rare:62 | ||||
chrX:123961537-123961787 | Rare:36 | ||||
chrX:130401874-130402015 | Common:2; Rare:42 |