| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:7927377-7927511 | Common:1; Rare:34 | ||||
| chrX:7927704-7927770 | Rare:11 | ||||
| chrX:11111196-11111474 | Common:4; Rare:47 | ||||
| chrX:12975199-12975238 | Rare:7 | ||||
| chrX:12976067-12976355 | Common:2; Rare:62 | ||||
| chrX:13734524-13734878 | Common:3; Rare:104; Clinvar (benign):1 | ||||
| chrX:14029812-14029989 | Common:2; Rare:56 | ||||
| chrX:14873040-14873152 | Common:1; Rare:21 | ||||
| chrX:15335502-15335684 | Common:2; Rare:42; Clinvar (benign):1 | ||||
| chrX:15500577-15500844 | Common:1; Rare:40 | ||||
| chrX:15507156-15507360 | Rare:27 | ||||
| chrX:16712579-16712720 | Common:1; Rare:22 | ||||
| chrX:16719452-16719810 | Common:1; Rare:93 | ||||
| chrX:16786168-16786490 | Common:2; Rare:66 | ||||
| chrX:18984037-18984211 | Rare:41 |