| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:14873005-14873513 | Common:5; Rare:195; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:15269863-15270273 | Common:2; Rare:115 | ||||
| chrX:15493204-15493437 | Common:2; Rare:71 | ||||
| chrX:15790401-15790535 | Rare:34 | ||||
| chrX:15854742-15855050 | Rare:127 | ||||
| chrX:16712521-16712727 | Common:2; Rare:51 | ||||
| chrX:16719426-16719699 | Rare:148 | ||||
| chrX:16786147-16786553 | Common:4; Rare:158 | ||||
| chrX:16870206-16870705 | Common:6; Rare:223 | ||||
| chrX:17736920-17737608 | Common:11; Rare:125 | ||||
| chrX:18425273-18425675 | Common:3; Rare:93; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:18984015-18984275 | Common:1; Rare:90 | ||||
| chrX:18984490-18984880 | Rare:118 | ||||
| chrX:19343677-19344033 | Common:12; Rare:194; Clinvar (benign):2 | ||||
| chrX:19887508-19888051 | Rare:134 |