| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132488936-132489171 | Rare:49 | ||||
| chrX:134807087-134807220 | Rare:23 | ||||
| chrX:134990869-134991021 | Rare:23 | ||||
| chrX:135032011-135032400 | Common:1; Rare:82 | ||||
| chrX:135052096-135052369 | Common:2; Rare:76 | ||||
| chrX:135344626-135344813 | Common:1; Rare:34 | ||||
| chrX:135973653-135973827 | Rare:61 | ||||
| chrX:136196980-136197068 | Rare:14 | ||||
| chrX:141177061-141177299 | Common:1; Rare:31 | ||||
| chrX:149505214-149505456 | Rare:72 | ||||
| chrX:149540811-149541059 | Common:4; Rare:46 | ||||
| chrX:149938407-149938637 | Common:1; Rare:58 | ||||
| chrX:150568310-150568660 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chrX:151396885-151397278 | Common:5; Rare:170 | ||||
| chrX:152830699-152831098 | Common:2; Rare:70 |