| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:19887537-19887600 | Rare:2 | ||||
| chrX:20141798-20142120 | Common:1; Rare:65 | ||||
| chrX:21374262-21374473 | Common:1; Rare:50 | ||||
| chrX:23782813-23783285 | Common:6; Rare:91 | ||||
| chrX:23783359-23783580 | Common:1; Rare:52 | ||||
| chrX:23784433-23784677 | Common:1; Rare:15 | ||||
| chrX:24054898-24055009 | Rare:43 | ||||
| chrX:24693751-24693927 | Common:1; Rare:24 | ||||
| chrX:30577740-30577899 | Common:1; Rare:17 | ||||
| chrX:30577914-30577957 | Rare:4 | ||||
| chrX:37847504-37847660 | Rare:40 | ||||
| chrX:40580726-40581021 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chrX:40735806-40736034 | Common:1; Rare:44 | ||||
| chrX:41333789-41334227 | Common:5; Rare:118 | ||||
| chrX:41334395-41334635 | Common:2; Rare:91 |