| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119236581-119236636 | Rare:16 | ||||
| chrX:119468206-119468501 | Common:3; Rare:98 | ||||
| chrX:119574349-119574603 | Rare:58 | ||||
| chrX:119791584-119791978 | Common:2; Rare:107 | ||||
| chrX:119871638-119871927 | Common:1; Rare:62; Clinvar (benign):3 | ||||
| chrX:120559855-120560114 | Rare:41 | ||||
| chrX:120560434-120560845 | Rare:62; Clinvar:2 | ||||
| chrX:120604031-120604154 | Rare:26 | ||||
| chrX:120604623-120604753 | Rare:9 | ||||
| chrX:123733025-123733112 | Rare:15 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961554-123961819 | Rare:40 | ||||
| chrX:129905981-129906205 | Rare:61 | ||||
| chrX:130339786-130339962 | Rare:25 | ||||
| chrX:132217734-132218012 | Common:1; Rare:36 |