| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:76172768-76173163 | Rare:77 | ||||
| chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77899268-77899539 | Rare:67; Clinvar (benign):1 | ||||
| chrX:78103950-78104319 | Common:4; Rare:137 | ||||
| chrX:78327532-78327674 | Rare:24 | ||||
| chrX:79367276-79367479 | Common:1; Rare:36 | ||||
| chrX:79367506-79367857 | Common:1; Rare:63 | ||||
| chrX:81201876-81202250 | Rare:62 | ||||
| chrX:81202312-81202675 | Common:2; Rare:49 | ||||
| chrX:85003773-85003909 | Common:1; Rare:29 | ||||
| chrX:86047516-86047643 | Common:1; Rare:25 | ||||
| chrX:87517597-87517952 | Common:2; Rare:70 | ||||
| chrX:100644048-100644284 | Common:1; Rare:29 | ||||
| chrX:100820279-100820446 | Common:2; Rare:39 | ||||
| chrX:101052071-101052237 | Rare:20 |