| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:72273230-72273633 | Common:1; Rare:66 | ||||
| chrX:72305824-72306156 | Common:1; Rare:42 | ||||
| chrX:72306896-72307092 | Rare:33 | ||||
| chrX:72307138-72307260 | Rare:19 | ||||
| chrX:72714128-72714350 | Rare:43 | ||||
| chrX:73563070-73563317 | Common:1; Rare:33 | ||||
| chrX:74614377-74614833 | Common:1; Rare:99 | ||||
| chrX:74925015-74925082 | Rare:18 | ||||
| chrX:75156020-75156388 | Common:3; Rare:98; Clinvar (benign):2 | ||||
| chrX:75273986-75274234 | Rare:35 | ||||
| chrX:75274645-75274702 | Common:1; Rare:10 | ||||
| chrX:75523013-75523225 | Common:1; Rare:45 | ||||
| chrX:75523239-75523281 | Rare:3 | ||||
| chrX:76172990-76173168 | Rare:48 | ||||
| chrX:77786171-77786248 | Common:1; Rare:14 |