| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961536-123961843 | Rare:43 | ||||
| chrX:129523120-129523666 | Common:5; Rare:134 | ||||
| chrX:129843790-129844034 | Common:1; Rare:31 | ||||
| chrX:129905998-129906213 | Rare:59 | ||||
| chrX:129982323-129982647 | Common:1; Rare:47 | ||||
| chrX:130165657-130165961 | Rare:65; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171780-130172080 | Common:2; Rare:75 | ||||
| chrX:130339795-130339993 | Rare:31 | ||||
| chrX:130401862-130402061 | Common:3; Rare:56 | ||||
| chrX:132023246-132023309 | Rare:16 | ||||
| chrX:132217823-132218012 | Rare:30 | ||||
| chrX:132218021-132218278 | Rare:27 | ||||
| chrX:134373093-134373472 | Common:5; Rare:91 | ||||
| chrX:134797181-134797304 | Rare:22 | ||||
| chrX:134807086-134807250 | Rare:25 |