| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:12975005-12975166 | Common:1; Rare:40 | ||||
| chrX:12976055-12976354 | Common:2; Rare:64 | ||||
| chrX:13734551-13734870 | Common:3; Rare:93; Clinvar (benign):1 | ||||
| chrX:14029777-14030099 | Common:3; Rare:82 | ||||
| chrX:14873035-14873469 | Common:1; Rare:80 | ||||
| chrX:15335511-15335818 | Common:3; Rare:63; Clinvar (benign):1 | ||||
| chrX:15790394-15790570 | Rare:41 | ||||
| chrX:16719472-16719655 | Rare:52 | ||||
| chrX:16786166-16786570 | Common:3; Rare:89 | ||||
| chrX:18984094-18984211 | Rare:24 | ||||
| chrX:19343652-19344002 | Common:6; Rare:96 | ||||
| chrX:20141761-20142071 | Common:1; Rare:66 | ||||
| chrX:21940649-21940792 | Common:1; Rare:38 | ||||
| chrX:23667375-23667580 | Common:2; Rare:66 | ||||
| chrX:23782884-23783195 | Common:5; Rare:60 |