Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:136644473-136644639 | Common:1; Rare:38 | ||||
chr9:136660380-136660563 | Rare:40 | ||||
chr9:136671687-136672009 | Common:1; Rare:94 | ||||
chr9:136839336-136839772 | Common:1; Rare:181 | ||||
chrM:15866-16093 | |||||
chrX:2609154-2609257 | Rare:32 | ||||
chrX:15675080-15675093 | Rare:2 | ||||
chrX:15675096-15675140 | Rare:15 | ||||
chrX:15675288-15675478 | Common:5; Rare:34 | ||||
chrX:15675601-15675735 | Common:1; Rare:25 | ||||
chrX:33726301-33726397 | Rare:18 | ||||
chrX:45769935-45770224 | Common:2; Rare:35 | ||||
chrX:47129753-47129904 | Common:1; Rare:13 | ||||
chrX:48522498-48522562 | Rare:10 | ||||
chrX:48901715-48901958 | Common:1; Rare:31; Clinvar (benign):1 |