| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135973662-135973818 | Rare:55 | ||||
| chrX:135973955-135974017 | Common:1; Rare:18 | ||||
| chrX:136197031-136197066 | Rare:1 | ||||
| chrX:136880596-136880744 | Common:1; Rare:39 | ||||
| chrX:136880757-136880882 | Rare:24 | ||||
| chrX:141177069-141177314 | Common:1; Rare:31 | ||||
| chrX:149504259-149504467 | Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:149505147-149505438 | Rare:82 | ||||
| chrX:149540411-149540615 | Common:2; Rare:22 | ||||
| chrX:149540799-149541059 | Common:4; Rare:49 | ||||
| chrX:149937872-149937941 | Common:1; Rare:19 | ||||
| chrX:149938434-149938667 | Common:2; Rare:57 | ||||
| chrX:150898576-150898911 | Common:3; Rare:93 | ||||
| chrX:151397057-151397261 | Common:4; Rare:102 | ||||
| chrX:152830712-152831095 | Common:2; Rare:67 |