| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:129843795-129844036 | Common:1; Rare:31 | ||||
| chrX:129905923-129906231 | Rare:79 | ||||
| chrX:130110422-130110630 | Rare:49 | ||||
| chrX:130165634-130165927 | Rare:59; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339782-130339976 | Rare:29 | ||||
| chrX:130401868-130402061 | Common:2; Rare:55 | ||||
| chrX:132023124-132023407 | Rare:63 | ||||
| chrX:132218040-132218248 | Rare:14 | ||||
| chrX:134373143-134373451 | Common:4; Rare:64 | ||||
| chrX:134460055-134460303 | Common:3; Rare:69 | ||||
| chrX:134797135-134797426 | Rare:48 | ||||
| chrX:134807141-134807261 | Rare:21 | ||||
| chrX:134915194-134915403 | Common:1; Rare:29 | ||||
| chrX:135032155-135032389 | Common:1; Rare:56 | ||||
| chrX:135052090-135052307 | Common:2; Rare:68 |