| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:129540231-129540363 | Common:1; Rare:32 | ||||
| chrX:129843794-129844080 | Common:1; Rare:40 | ||||
| chrX:129905957-129906224 | Rare:68 | ||||
| chrX:130165822-130165968 | Rare:29; Clinvar (benign):1 | ||||
| chrX:130401873-130402035 | Common:2; Rare:49 | ||||
| chrX:132023172-132023345 | Rare:41 | ||||
| chrX:132217726-132218291 | Common:1; Rare:71 | ||||
| chrX:132219430-132219611 | Rare:22 | ||||
| chrX:132413573-132413626 | Rare:6 | ||||
| chrX:135022468-135022560 | Rare:32 | ||||
| chrX:135032150-135032419 | Common:1; Rare:62 | ||||
| chrX:135032471-135032789 | Rare:59 | ||||
| chrX:135052067-135052369 | Common:2; Rare:89 | ||||
| chrX:135344601-135344818 | Common:2; Rare:38 | ||||
| chrX:135520375-135520665 | Rare:31 |