| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:129523441-129523677 | Common:3; Rare:34 | ||||
| chrX:129654421-129654568 | Rare:37 | ||||
| chrX:129843784-129844049 | Common:1; Rare:34 | ||||
| chrX:129905846-129906209 | Rare:83 | ||||
| chrX:129980829-129981513 | Common:1; Rare:115 | ||||
| chrX:129982271-129982665 | Common:1; Rare:57 | ||||
| chrX:130165691-130165997 | Rare:68; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130170830-130171160 | Common:4; Rare:59 | ||||
| chrX:130268317-130268457 | Rare:21 | ||||
| chrX:130268778-130269004 | Common:1; Rare:67 | ||||
| chrX:130339737-130339971 | Rare:40 | ||||
| chrX:130401856-130402035 | Common:3; Rare:55 | ||||
| chrX:130902693-130903012 | Rare:39 | ||||
| chrX:130903166-130903581 | Common:2; Rare:73 | ||||
| chrX:131289181-131289581 | Common:6; Rare:144 |