| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13688871-13689167 | Rare:62 | ||||
| chrX:13734263-13734405 | Rare:23 | ||||
| chrX:13734524-13734876 | Common:3; Rare:103; Clinvar (benign):1 | ||||
| chrX:14029833-14030046 | Common:3; Rare:65 | ||||
| chrX:14873027-14873431 | Common:1; Rare:76 | ||||
| chrX:15335511-15335765 | Common:3; Rare:54; Clinvar (benign):1 | ||||
| chrX:15790389-15790570 | Rare:42 | ||||
| chrX:16719494-16719655 | Rare:47 | ||||
| chrX:16786143-16786558 | Common:3; Rare:88 | ||||
| chrX:16870239-16870763 | Common:3; Rare:117 | ||||
| chrX:19343700-19343997 | Common:6; Rare:83 | ||||
| chrX:20141757-20142117 | Common:1; Rare:81 | ||||
| chrX:21940542-21940756 | Common:2; Rare:60 | ||||
| chrX:23667386-23667565 | Common:2; Rare:58 | ||||
| chrX:23782940-23783230 | Common:5; Rare:60 |