| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153794273-153794749 | Common:1; Rare:145; Clinvar (benign):2 | ||||
| chrX:153944588-153944743 | Common:2; Rare:34 | ||||
| chrX:153970913-153971278 | Rare:78 | ||||
| chrX:153972417-153972790 | Common:2; Rare:115 | ||||
| chrX:154352383-154352672 | Rare:55; Clinvar:3; Clinvar (benign):9 | ||||
| chrX:154359325-154359507 | Rare:42; Clinvar:2; Clinvar (benign):5 | ||||
| chrX:154374580-154374810 | Rare:43 | ||||
| chrX:154398826-154399026 | Common:2; Rare:44 | ||||
| chrX:154409146-154409427 | Rare:46 | ||||
| chrX:154428446-154428707 | Common:2; Rare:47 | ||||
| chrX:154486559-154486772 | Rare:34 | ||||
| chrX:154490614-154490791 | Common:2; Rare:45 | ||||
| chrX:154516078-154516536 | Common:4; Rare:89 | ||||
| chrX:154541191-154541312 | Rare:20 | ||||
| chrX:154542088-154542275 | Rare:33 |