| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153794319-153794672 | Common:1; Rare:113; Clinvar (benign):2 | ||||
| chrX:153934883-153935359 | Common:2; Rare:104 | ||||
| chrX:153971157-153971274 | Rare:27 | ||||
| chrX:153971564-153971616 | Rare:9 | ||||
| chrX:154019831-154020027 | Rare:39 | ||||
| chrX:154354615-154355075 | Common:1; Rare:122; Clinvar:12; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chrX:154364820-154365185 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):12 | ||||
| chrX:154374509-154374764 | Common:1; Rare:49 | ||||
| chrX:154398812-154399035 | Common:3; Rare:50 | ||||
| chrX:154409182-154409469 | Rare:43 | ||||
| chrX:154411249-154411576 | Rare:57 | ||||
| chrX:154428434-154428849 | Common:3; Rare:91; Clinvar:1 | ||||
| chrX:154437134-154437261 | Rare:55 | ||||
| chrX:154478775-154478851 | Common:2; Rare:27 | ||||
| chrX:154486554-154486783 | Rare:37 |