| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:14873040-14873474 | Common:1; Rare:81 | ||||
| chrX:15500583-15500892 | Common:2; Rare:43 | ||||
| chrX:15790404-15790526 | Rare:34 | ||||
| chrX:15854705-15854909 | Rare:40 | ||||
| chrX:16712650-16712720 | Rare:11 | ||||
| chrX:16719279-16719722 | Rare:109 | ||||
| chrX:18984046-18984237 | Rare:44 | ||||
| chrX:19343701-19344040 | Common:6; Rare:95; Clinvar (benign):1 | ||||
| chrX:23782948-23783423 | Common:5; Rare:104 | ||||
| chrX:23784534-23784678 | Common:1; Rare:6 | ||||
| chrX:23785310-23785560 | Common:1; Rare:46 | ||||
| chrX:23907706-23908070 | Common:1; Rare:78 | ||||
| chrX:24054898-24054983 | Rare:28 | ||||
| chrX:24465044-24465347 | Common:4; Rare:87 | ||||
| chrX:33211440-33211758 | Rare:52; Clinvar:3; Clinvar (benign):2 |