Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:16719512-16719671 | Rare:48 | ||||
chrX:70289875-70290099 | Rare:42 | ||||
chrX:81201889-81202179 | Rare:49 | ||||
chrX:101407897-101408238 | Common:5; Rare:61; Clinvar (benign):9 | ||||
chrX:107717054-107717183 | Rare:19 | ||||
chrX:119871756-119871862 | Rare:17 | ||||
chrX:135973751-135973775 | Rare:4 | ||||
chrX:152830712-152831028 | Common:1; Rare:57 | ||||
chrX:153794330-153794684 | Common:1; Rare:109; Clinvar (benign):2 |