| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:134796542-134796796 | Rare:18 | ||||
| chrX:134797081-134797374 | Rare:50 | ||||
| chrX:134807083-134807223 | Rare:24 | ||||
| chrX:134915200-134915494 | Common:1; Rare:46 | ||||
| chrX:135021690-135022060 | Common:2; Rare:114 | ||||
| chrX:135022469-135022630 | Rare:40 | ||||
| chrX:135032124-135032383 | Common:1; Rare:59 | ||||
| chrX:135052132-135052351 | Common:2; Rare:55 | ||||
| chrX:135098670-135099110 | Common:2; Rare:92 | ||||
| chrX:135344005-135344258 | Common:1; Rare:46 | ||||
| chrX:135344626-135344821 | Common:1; Rare:36 | ||||
| chrX:135421633-135421785 | Rare:20 | ||||
| chrX:135520459-135520723 | Rare:41 | ||||
| chrX:135973673-135973884 | Rare:70 | ||||
| chrX:135985248-135985503 | Rare:62; Clinvar (benign):4 |