| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:149939942-149940138 | Common:1; Rare:42 | ||||
| chrX:154351909-154352201 | Common:1; Rare:63; Clinvar:8; Clinvar (benign):2 | ||||
| chrX:154362249-154362462 | Rare:54; Clinvar:5; Clinvar (benign):2 | ||||
| chrY:3002642-3002905 | Rare:1 | ||||
| chrY:12662009-12662271 | Rare:2 | ||||
| chrY:19077346-19077493 | Rare:1 |