Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:16720363-16720654 | Rare:38 | ||||
chrX:16728688-16728985 | Common:2; Rare:23 | ||||
chrX:16737648-16737726 | Rare:10 | ||||
chrX:16755686-16755959 | Rare:32 | ||||
chrX:21978881-21979159 | Rare:41; Clinvar (benign):1 | ||||
chrX:21993874-21994159 | Rare:38 | ||||
chrX:23874837-23875020 | Common:2; Rare:23 | ||||
chrX:24008912-24008972 | Common:1; Rare:7 | ||||
chrX:24062356-24062448 | Rare:14 | ||||
chrX:24075090-24075320 | Common:1; Rare:27 | ||||
chrX:24207449-24207816 | Common:1; Rare:54 | ||||
chrX:29660048-29660212 | Common:4; Rare:27 | ||||
chrX:39786955-39786974 | Rare:1 | ||||
chrX:41215438-41215637 | Common:1; Rare:22 | ||||
chrX:44741777-44741898 | Common:1; Rare:13 |