| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:15790415-15790575 | Rare:36 | ||||
| chrX:16712618-16712744 | Common:2; Rare:19 | ||||
| chrX:16719372-16719690 | Rare:81 | ||||
| chrX:16786168-16786554 | Common:3; Rare:86 | ||||
| chrX:19343693-19344004 | Common:6; Rare:88 | ||||
| chrX:19670887-19670990 | Rare:21 | ||||
| chrX:20141656-20141879 | Common:1; Rare:62 | ||||
| chrX:21940607-21940864 | Common:2; Rare:64 | ||||
| chrX:23667319-23667572 | Common:2; Rare:80 | ||||
| chrX:23743145-23743398 | Common:5; Rare:47 | ||||
| chrX:23782984-23783360 | Common:5; Rare:79 | ||||
| chrX:23907714-23907998 | Common:1; Rare:57 | ||||
| chrX:24054619-24055022 | Common:1; Rare:94 | ||||
| chrX:37847495-37847776 | Common:1; Rare:60 | ||||
| chrX:40580729-40581041 | Common:5; Rare:76; Clinvar (benign):3 |