| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135022487-135022591 | Rare:28 | ||||
| chrX:135032246-135032375 | Rare:30 | ||||
| chrX:135052118-135052248 | Common:1; Rare:36 | ||||
| chrX:135344580-135344823 | Common:2; Rare:44 | ||||
| chrX:135973704-135973785 | Rare:26 | ||||
| chrX:136251326-136251476 | Rare:47 | ||||
| chrX:141177076-141177322 | Common:1; Rare:33 | ||||
| chrX:149540924-149541012 | Common:2; Rare:13 | ||||
| chrX:149938440-149938639 | Common:2; Rare:50 | ||||
| chrX:150898545-150898911 | Common:4; Rare:99 | ||||
| chrX:151396957-151397251 | Common:5; Rare:132 | ||||
| chrX:151974651-151974777 | Rare:43 | ||||
| chrX:152830708-152831095 | Common:2; Rare:68 | ||||
| chrX:153794313-153794690 | Common:1; Rare:116; Clinvar (benign):2 | ||||
| chrX:153944606-153944749 | Common:2; Rare:33 |