| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:11427728-11427915 | Rare:41 | ||||
| chrX:11759432-11759665 | Rare:29 | ||||
| chrX:12976063-12976361 | Common:2; Rare:63 | ||||
| chrX:13652964-13653188 | Rare:50 | ||||
| chrX:13688969-13689250 | Common:2; Rare:77 | ||||
| chrX:13734523-13734854 | Common:3; Rare:100; Clinvar (benign):1 | ||||
| chrX:14029801-14030082 | Common:3; Rare:77 | ||||
| chrX:14529394-14529888 | Common:2; Rare:65 | ||||
| chrX:14873031-14873533 | Common:2; Rare:98 | ||||
| chrX:15335509-15335674 | Common:2; Rare:38; Clinvar (benign):1 | ||||
| chrX:15790426-15790570 | Rare:33 | ||||
| chrX:16719539-16719691 | Rare:46 | ||||
| chrX:16786108-16786550 | Common:3; Rare:94 | ||||
| chrX:16870209-16870650 | Common:3; Rare:102 | ||||
| chrX:19343693-19344006 | Common:6; Rare:88 |