| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:12975911-12976095 | Common:3; Rare:30 | ||||
| chrX:13653061-13653196 | Rare:28 | ||||
| chrX:13689000-13689276 | Common:2; Rare:79 | ||||
| chrX:13734540-13734859 | Common:3; Rare:96; Clinvar (benign):1 | ||||
| chrX:14029800-14030042 | Common:3; Rare:73 | ||||
| chrX:14873002-14873535 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:15854725-15854927 | Rare:44 | ||||
| chrX:16719353-16719751 | Rare:99 | ||||
| chrX:16786215-16786488 | Common:1; Rare:54 | ||||
| chrX:16870039-16870429 | Common:2; Rare:85 | ||||
| chrX:18984049-18984203 | Rare:36 | ||||
| chrX:18984229-18984459 | Common:1; Rare:43 | ||||
| chrX:18984536-18984683 | Rare:32 | ||||
| chrX:19670867-19671178 | Common:1; Rare:50 | ||||
| chrX:19887529-19887600 | Rare:2 |