| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:11111132-11111382 | Common:4; Rare:54 | ||||
| chrX:11759469-11759687 | Rare:27 | ||||
| chrX:12791300-12791466 | Rare:33 | ||||
| chrX:12975527-12975649 | Common:1; Rare:33 | ||||
| chrX:12976012-12976361 | Common:3; Rare:71 | ||||
| chrX:13689000-13689226 | Common:2; Rare:67 | ||||
| chrX:13734564-13734859 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chrX:14873027-14873463 | Common:1; Rare:83 | ||||
| chrX:15270035-15270306 | Common:2; Rare:41 | ||||
| chrX:16719402-16719718 | Rare:87 | ||||
| chrX:19343707-19344031 | Common:6; Rare:91; Clinvar (benign):1 | ||||
| chrX:19670876-19670979 | Rare:22 | ||||
| chrX:20141757-20142071 | Common:1; Rare:69 | ||||
| chrX:20267048-20267139 | Rare:19 | ||||
| chrX:23667367-23667567 | Common:2; Rare:63 |