| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:17374917-17375267 | Common:4; Rare:46 | ||||
| chrX:17737031-17737102 | Common:1; Rare:15 | ||||
| chrX:17737107-17737628 | Common:5; Rare:59 | ||||
| chrX:17861294-17861531 | Common:1; Rare:27 | ||||
| chrX:18354639-18354745 | Common:1; Rare:22 | ||||
| chrX:18425271-18425660 | Common:3; Rare:90; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:18442119-18442233 | Common:1; Rare:22 | ||||
| chrX:18690832-18690992 | Rare:22 | ||||
| chrX:18984037-18984211 | Rare:41 | ||||
| chrX:19343707-19344018 | Common:6; Rare:85; Clinvar (benign):1 | ||||
| chrX:20141664-20142043 | Common:1; Rare:86 | ||||
| chrX:21374116-21374447 | Common:1; Rare:78 | ||||
| chrX:21839490-21839663 | Rare:39 | ||||
| chrX:21856148-21856359 | Common:1; Rare:69 | ||||
| chrX:21940649-21940858 | Common:1; Rare:49 |