| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56563382-56563674 | Common:1; Rare:62; Clinvar:1 | ||||
| chrX:56729458-56729578 | Common:1; Rare:15 | ||||
| chrX:57121422-57121606 | Common:1; Rare:43 | ||||
| chrX:63351274-63351567 | Common:2; Rare:70 | ||||
| chrX:63755031-63755138 | Rare:23 | ||||
| chrX:64205663-64206017 | Common:1; Rare:65 | ||||
| chrX:65034697-65034921 | Common:1; Rare:42 | ||||
| chrX:65035182-65035234 | Rare:7 | ||||
| chrX:65667538-65667853 | Rare:54 | ||||
| chrX:66639025-66639343 | Rare:22 | ||||
| chrX:68498961-68499078 | Rare:27 | ||||
| chrX:68693471-68693692 | Rare:55 | ||||
| chrX:68828837-68829040 | Rare:42 | ||||
| chrX:70289865-70289987 | Rare:28 | ||||
| chrX:70452341-70452616 | Common:2; Rare:53; Clinvar (benign):1 |