| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961545-123961856 | Rare:45 | ||||
| chrX:129523217-129523602 | Common:4; Rare:100 | ||||
| chrX:129843795-129844078 | Common:1; Rare:39 | ||||
| chrX:129905938-129906201 | Rare:68 | ||||
| chrX:129982363-129982636 | Common:1; Rare:39 | ||||
| chrX:130165671-130165990 | Rare:69; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130401679-130402059 | Common:3; Rare:79 | ||||
| chrX:132023153-132023345 | Rare:46 | ||||
| chrX:132217762-132218012 | Common:1; Rare:33 | ||||
| chrX:132489036-132489261 | Rare:32 | ||||
| chrX:132490014-132490043 | Rare:5 | ||||
| chrX:134373103-134373424 | Common:5; Rare:83 | ||||
| chrX:134915197-134915403 | Common:1; Rare:29 | ||||
| chrX:135022468-135022554 | Rare:27 | ||||
| chrX:135032155-135032383 | Common:1; Rare:54 |