| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135344625-135344830 | Common:1; Rare:40 | ||||
| chrX:135520520-135520834 | Rare:51 | ||||
| chrX:135973671-135973835 | Rare:59 | ||||
| chrX:135985311-135985503 | Rare:51; Clinvar (benign):4 | ||||
| chrX:136880622-136880944 | Common:1; Rare:81 | ||||
| chrX:138711707-138711835 | Common:1; Rare:22 | ||||
| chrX:139204989-139205141 | Rare:21 | ||||
| chrX:139205518-139205648 | Rare:16 | ||||
| chrX:139933025-139933277 | Rare:46 | ||||
| chrX:141177065-141177321 | Common:1; Rare:34 | ||||
| chrX:147911819-147912173 | Common:3; Rare:115 | ||||
| chrX:149505223-149505399 | Rare:54 | ||||
| chrX:149540806-149541048 | Common:4; Rare:46 | ||||
| chrX:149938407-149938665 | Common:2; Rare:65 | ||||
| chrX:150568320-150568660 | Common:1; Rare:75; Clinvar (benign):1 |