Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:107652010-107652140 | Rare:17 | ||||
chrX:107674145-107674340 | Rare:20 | ||||
chrX:107676876-107677169 | Common:1; Rare:38 | ||||
chrX:123514506-123514710 | Common:1; Rare:26 | ||||
chrX:135032978-135033039 | Rare:10 | ||||
chrX:154349400-154349683 | Common:2; Rare:73; Clinvar:10; Clinvar (benign):11 |