| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13734526-13734854 | Common:3; Rare:99; Clinvar (benign):1 | ||||
| chrX:14873106-14873431 | Common:1; Rare:62 | ||||
| chrX:16719444-16719690 | Rare:71 | ||||
| chrX:20141773-20142071 | Common:1; Rare:61 | ||||
| chrX:23667317-23667581 | Common:2; Rare:82 | ||||
| chrX:23782984-23783334 | Common:5; Rare:73 | ||||
| chrX:23907706-23908029 | Common:1; Rare:67 | ||||
| chrX:24054890-24054987 | Rare:36 | ||||
| chrX:24149638-24149744 | Rare:20 | ||||
| chrX:24465060-24465329 | Common:4; Rare:76 | ||||
| chrX:24693770-24693956 | Common:1; Rare:32 | ||||
| chrX:30653134-30653436 | Common:2; Rare:79 | ||||
| chrX:40580735-40581011 | Common:4; Rare:66 | ||||
| chrX:40735814-40735878 | Common:1; Rare:13 | ||||
| chrX:41334056-41334185 | Common:1; Rare:28 |