| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:1392050-1392383 | Common:6; Rare:145 | ||||
| chrX:2691025-2691421 | Common:14; Rare:140 | ||||
| chrX:16786349-16786483 | Rare:30 | ||||
| chrX:21940513-21940787 | Common:2; Rare:76 | ||||
| chrX:24054901-24055021 | Rare:43 | ||||
| chrX:38220815-38221047 | Rare:52 | ||||
| chrX:46545391-46545566 | Rare:42 | ||||
| chrX:47144684-47144794 | Rare:19 | ||||
| chrX:47483159-47483234 | Common:1; Rare:12 | ||||
| chrX:47659079-47659274 | Rare:56 | ||||
| chrX:48508848-48509075 | Common:1; Rare:45 | ||||
| chrX:48527013-48527276 | Rare:46; Clinvar (benign):2 | ||||
| chrX:48574312-48574565 | Common:1; Rare:81 | ||||
| chrX:48574876-48575019 | Rare:40 | ||||
| chrX:48898153-48898274 | Common:1; Rare:20 |