| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:151396964-151397264 | Common:5; Rare:134 | ||||
| chrX:152830706-152831070 | Common:2; Rare:68 | ||||
| chrX:152941656-152941698 | Common:1; Rare:11 | ||||
| chrX:153599071-153599363 | Common:13; Rare:57 | ||||
| chrX:153724570-153724883 | Common:1; Rare:66 | ||||
| chrX:153794323-153794699 | Common:1; Rare:118; Clinvar (benign):2 | ||||
| chrX:153971168-153971278 | Rare:25 | ||||
| chrX:154409215-154409315 | Rare:17 | ||||
| chrX:154428457-154428689 | Common:2; Rare:40 | ||||
| chrX:154516156-154516536 | Common:4; Rare:79 | ||||
| chrX:154547567-154547639 | Common:1; Rare:16; Clinvar (benign):1 | ||||
| chrX:154805486-154805544 | Rare:8 | ||||
| chrX:155026897-155026947 | Rare:15 | ||||
| chrX:155026949-155027061 | Rare:31 |