| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:12975005-12975177 | Common:2; Rare:40 | ||||
| chrX:12975647-12975814 | Common:1; Rare:22 | ||||
| chrX:12975906-12976204 | Common:4; Rare:54 | ||||
| chrX:13734584-13734796 | Common:3; Rare:63; Clinvar (benign):1 | ||||
| chrX:14029875-14030020 | Common:2; Rare:40 | ||||
| chrX:14873035-14873263 | Common:1; Rare:50 | ||||
| chrX:15749790-15749931 | Rare:11 | ||||
| chrX:15790408-15790575 | Rare:38 | ||||
| chrX:16719328-16719697 | Rare:90 | ||||
| chrX:16786287-16786493 | Common:1; Rare:47 | ||||
| chrX:18984322-18984463 | Rare:29 | ||||
| chrX:19887524-19887600 | Rare:2 | ||||
| chrX:20141801-20142117 | Common:1; Rare:60 | ||||
| chrX:20267040-20267200 | Common:1; Rare:31 | ||||
| chrX:21940607-21940786 | Common:2; Rare:51 |