| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135052096-135052301 | Common:2; Rare:64 | ||||
| chrX:135344611-135344823 | Common:1; Rare:41 | ||||
| chrX:135973679-135973850 | Rare:60 | ||||
| chrX:135973976-135974006 | Rare:6 | ||||
| chrX:135985399-135985532 | Rare:45; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chrX:136146778-136146862 | Rare:24 | ||||
| chrX:136147242-136147608 | Common:4; Rare:49 | ||||
| chrX:136497076-136497425 | Common:3; Rare:89 | ||||
| chrX:136767314-136767565 | Common:3; Rare:37 | ||||
| chrX:136880596-136880878 | Common:1; Rare:66 | ||||
| chrX:138711652-138711827 | Common:2; Rare:35 | ||||
| chrX:139203451-139203596 | Common:2; Rare:18 | ||||
| chrX:139933048-139933162 | Rare:20 | ||||
| chrX:141177065-141177325 | Common:1; Rare:34 | ||||
| chrX:143634989-143635179 | Rare:27 |