| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70479022-70479263 | Common:1; Rare:47; Clinvar:1 | ||||
| chrX:70479348-70479414 | Rare:8 | ||||
| chrX:71283430-71283720 | Rare:46 | ||||
| chrX:71532820-71533152 | Rare:68 | ||||
| chrX:73563231-73563324 | Rare:13 | ||||
| chrX:75156018-75156039 | Common:1; Rare:3 | ||||
| chrX:75156239-75156315 | Common:1; Rare:25 | ||||
| chrX:75523018-75523151 | Rare:29 | ||||
| chrX:76172791-76173134 | Rare:62 | ||||
| chrX:77895412-77895741 | Rare:92; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103971-78104326 | Common:4; Rare:131 | ||||
| chrX:79367307-79367438 | Common:1; Rare:25 | ||||
| chrX:80335310-80335385 | Common:2; Rare:13 | ||||
| chrX:81201889-81202250 | Rare:62 | ||||
| chrX:100644038-100644236 | Rare:28 |