| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56995499-56995625 | Common:1; Rare:25 | ||||
| chrX:63351310-63351569 | Common:2; Rare:61 | ||||
| chrX:66639025-66639154 | Rare:7 | ||||
| chrX:68498984-68499059 | Rare:16 | ||||
| chrX:68828837-68829034 | Rare:40 | ||||
| chrX:70289875-70290131 | Rare:49 | ||||
| chrX:71068313-71068675 | Common:2; Rare:83 | ||||
| chrX:71532912-71533115 | Rare:39 | ||||
| chrX:72079646-72079844 | Rare:32 | ||||
| chrX:72714198-72714404 | Common:1; Rare:48 | ||||
| chrX:76172928-76173141 | Rare:45 | ||||
| chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103973-78104371 | Common:4; Rare:144 | ||||
| chrX:81201884-81202195 | Rare:52 | ||||
| chrX:87517909-87518146 | Common:2; Rare:51 |