| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135032152-135032394 | Common:1; Rare:58 | ||||
| chrX:135032503-135032730 | Rare:33 | ||||
| chrX:135052096-135052372 | Common:2; Rare:76 | ||||
| chrX:135343999-135344243 | Common:1; Rare:43 | ||||
| chrX:135344625-135344823 | Common:1; Rare:38 | ||||
| chrX:135973679-135973835 | Rare:56 | ||||
| chrX:135985342-135985510 | Rare:50; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:136147266-136147597 | Common:4; Rare:45 | ||||
| chrX:136169343-136169750 | Common:2; Rare:48 | ||||
| chrX:136204463-136204982 | Rare:72 | ||||
| chrX:136497056-136497418 | Common:3; Rare:92 | ||||
| chrX:136767154-136767404 | Common:1; Rare:40 | ||||
| chrX:138711303-138711492 | Common:2; Rare:49 | ||||
| chrX:138711652-138711855 | Common:2; Rare:41 | ||||
| chrX:139205019-139205161 | Rare:25 |