| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13734543-13734832 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chrX:14873203-14873463 | Rare:44 | ||||
| chrX:15270071-15270273 | Rare:34 | ||||
| chrX:15500616-15500866 | Common:1; Rare:39 | ||||
| chrX:16719444-16719718 | Rare:82 | ||||
| chrX:16786205-16786503 | Common:1; Rare:63 | ||||
| chrX:19670870-19671048 | Rare:33 | ||||
| chrX:20141741-20142099 | Common:1; Rare:81 | ||||
| chrX:20218840-20219039 | Rare:38 | ||||
| chrX:23782911-23783248 | Common:5; Rare:74 | ||||
| chrX:24054891-24055031 | Rare:50 | ||||
| chrX:37349155-37349411 | Common:2; Rare:41 | ||||
| chrX:37847517-37847677 | Common:1; Rare:40 | ||||
| chrX:38220714-38220945 | Common:3; Rare:66 | ||||
| chrX:38327445-38327649 | Rare:46 |