| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120604300-120604790 | Rare:108 | ||||
| chrX:120629932-120630322 | Common:8; Rare:146 | ||||
| chrX:123733007-123733189 | Rare:56; Clinvar (benign):1 | ||||
| chrX:123859905-123860515 | Common:2; Rare:205 | ||||
| chrX:123960279-123960783 | Rare:75 | ||||
| chrX:123961210-123961433 | Common:4; Rare:53 | ||||
| chrX:123961536-123961836 | Rare:42 | ||||
| chrX:129523344-129523763 | Common:8; Rare:120 | ||||
| chrX:129905923-129906213 | Rare:135 | ||||
| chrX:129982251-129982715 | Common:2; Rare:117 | ||||
| chrX:130110491-130110645 | Rare:36 | ||||
| chrX:130165644-130165964 | Rare:127; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chrX:130268891-130268998 | Common:1; Rare:71 | ||||
| chrX:130339729-130339986 | Rare:71 | ||||
| chrX:130401868-130402040 | Common:4; Rare:95 |