| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13653043-13653196 | Rare:34 | ||||
| chrX:13689000-13689197 | Rare:57 | ||||
| chrX:13734524-13735005 | Common:3; Rare:132; Clinvar (benign):1 | ||||
| chrX:14029792-14029975 | Common:1; Rare:58 | ||||
| chrX:14873040-14873470 | Common:1; Rare:80 | ||||
| chrX:15269879-15270229 | Common:1; Rare:53 | ||||
| chrX:15270237-15270267 | |||||
| chrX:15335494-15335700 | Common:3; Rare:49; Clinvar (benign):1 | ||||
| chrX:15493226-15493397 | Common:1; Rare:32 | ||||
| chrX:15790389-15790570 | Rare:42 | ||||
| chrX:15854721-15854932 | Rare:48 | ||||
| chrX:16167576-16167743 | Rare:33 | ||||
| chrX:16719468-16719776 | Rare:85 | ||||
| chrX:16786191-16786554 | Common:2; Rare:80 | ||||
| chrX:16870116-16870650 | Common:3; Rare:125 |