| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70478788-70479098 | Common:2; Rare:32 | ||||
| chrX:71111526-71111685 | Rare:18; Clinvar:2 | ||||
| chrX:71118659-71118775 | Rare:32; Clinvar (benign):2 | ||||
| chrX:71254103-71254238 | Common:1; Rare:24 | ||||
| chrX:71254667-71254818 | Common:1; Rare:13 | ||||
| chrX:71365896-71366256 | Common:4; Rare:66 | ||||
| chrX:72305910-72305990 | Rare:22 | ||||
| chrX:72307151-72307240 | Rare:13 | ||||
| chrX:73214690-73215005 | Common:1; Rare:47 | ||||
| chrX:73563055-73563324 | Common:1; Rare:36 | ||||
| chrX:74421294-74421572 | Common:1; Rare:67; Clinvar (benign):3 | ||||
| chrX:74614433-74614735 | Rare:57 | ||||
| chrX:75156018-75156399 | Common:3; Rare:100; Clinvar (benign):2 | ||||
| chrX:75273970-75274232 | Rare:37 | ||||
| chrX:75274636-75274733 | Common:1; Rare:16 |