| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135052086-135052290 | Common:2; Rare:65 | ||||
| chrX:135344626-135344812 | Common:1; Rare:34 | ||||
| chrX:135973722-135973870 | Rare:47 | ||||
| chrX:135985307-135985503 | Rare:52; Clinvar (benign):4 | ||||
| chrX:136880695-136880912 | Rare:48 | ||||
| chrX:141177061-141177423 | Common:2; Rare:60 | ||||
| chrX:149540874-149541094 | Common:3; Rare:40 | ||||
| chrX:149631719-149631875 | Common:1; Rare:47 | ||||
| chrX:149938440-149938626 | Common:1; Rare:48 | ||||
| chrX:150568305-150568643 | Common:1; Rare:69 | ||||
| chrX:150983058-150983373 | Common:3; Rare:66 | ||||
| chrX:151396877-151397286 | Common:6; Rare:175 | ||||
| chrX:151974674-151974913 | Common:1; Rare:67 | ||||
| chrX:152698649-152698805 | Rare:1 | ||||
| chrX:152830712-152831098 | Common:2; Rare:67 |