| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120561428-120561653 | Common:1; Rare:31 | ||||
| chrX:120603796-120604167 | Rare:70 | ||||
| chrX:120629932-120630282 | Common:4; Rare:68 | ||||
| chrX:123733009-123733174 | Rare:30; Clinvar (benign):1 | ||||
| chrX:123859710-123860066 | Common:2; Rare:53 | ||||
| chrX:123960376-123960742 | Rare:23 | ||||
| chrX:123960770-123960907 | Rare:19 | ||||
| chrX:123961264-123961434 | Common:2; Rare:22 | ||||
| chrX:123961528-123961843 | Rare:44 | ||||
| chrX:129523219-129523640 | Common:4; Rare:103 | ||||
| chrX:129843795-129844059 | Common:1; Rare:36 | ||||
| chrX:129906073-129906217 | Rare:34 | ||||
| chrX:130171750-130172080 | Common:2; Rare:78 | ||||
| chrX:130401873-130402023 | Common:2; Rare:45 | ||||
| chrX:132218006-132218287 | Rare:33 |