| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53683821-53683880 | Common:1; Rare:13 | ||||
| chrX:54530064-54530246 | Common:2; Rare:22 | ||||
| chrX:55161108-55161246 | Rare:41 | ||||
| chrX:57121476-57121607 | Common:1; Rare:31 | ||||
| chrX:68498965-68499056 | Rare:22 | ||||
| chrX:68828832-68829030 | Rare:40 | ||||
| chrX:70289892-70290106 | Rare:37 | ||||
| chrX:72027461-72027571 | Rare:12 | ||||
| chrX:75156277-75156369 | Common:2; Rare:24 | ||||
| chrX:77895412-77895741 | Rare:92; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201881-81202245 | Rare:62 | ||||
| chrX:87517849-87518074 | Common:1; Rare:51 | ||||
| chrX:101348711-101348804 | Common:2; Rare:11 | ||||
| chrX:101407960-101408274 | Common:2; Rare:48; Clinvar (benign):2 | ||||
| chrX:102651318-102651426 | Common:2; Rare:33 |