| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:77786105-77786357 | Common:1; Rare:33 | ||||
| chrX:77895412-77895741 | Rare:92; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103962-78104289 | Common:4; Rare:111 | ||||
| chrX:80335311-80335413 | Common:2; Rare:18 | ||||
| chrX:81201876-81202245 | Rare:62 | ||||
| chrX:85003712-85003915 | Common:2; Rare:34 | ||||
| chrX:100644181-100644284 | Common:1; Rare:13 | ||||
| chrX:100820268-100820414 | Common:2; Rare:30 | ||||
| chrX:101386156-101386247 | Rare:7 | ||||
| chrX:101407876-101408311 | Common:5; Rare:83; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:101622990-101623215 | Common:1; Rare:38 | ||||
| chrX:103276731-103276912 | Rare:23 | ||||
| chrX:103356393-103356580 | Common:3; Rare:22 | ||||
| chrX:103376448-103376607 | Common:1; Rare:24 | ||||
| chrX:103585445-103585670 | Common:3; Rare:45 |