| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135521625-135521969 | Common:3; Rare:39 | ||||
| chrX:136909267-136909480 | Rare:55 | ||||
| chrX:138635512-138635828 | Rare:32 | ||||
| chrX:142998821-142998908 | Rare:10 | ||||
| chrX:143094751-143094967 | Rare:32 | ||||
| chrX:143096342-143096539 | Common:1; Rare:24 | ||||
| chrX:153411345-153411487 | Common:2; Rare:44 | ||||
| chrX:154352022-154352198 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chrX:154364157-154364352 | Rare:42; Clinvar:1; Clinvar (benign):3 | ||||
| chrY:3002801-3002905 | Rare:1 | ||||
| chrY:7273875-7273999 | |||||
| chrY:7274767-7274855 | |||||
| chrY:12662203-12662548 | Rare:4 | ||||
| chrY:19075964-19076189 | Rare:2 | ||||
| chrY:19077115-19077165 |