| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154397605-154397720 | Common:1; Rare:22 | ||||
| chrX:154398210-154398542 | Common:3; Rare:123 | ||||
| chrX:154398798-154399051 | Common:4; Rare:59 | ||||
| chrX:154428457-154428712 | Common:2; Rare:46 | ||||
| chrX:154486571-154486743 | Rare:28 | ||||
| chrX:154490614-154490774 | Common:2; Rare:41 | ||||
| chrX:154515787-154515956 | Rare:25 | ||||
| chrX:154516156-154516511 | Common:4; Rare:74 | ||||
| chrX:154541067-154541323 | Rare:40 | ||||
| chrX:154541909-154542247 | Rare:54 | ||||
| chrX:154547567-154547639 | Common:1; Rare:16; Clinvar (benign):1 | ||||
| chrX:154805331-154805586 | Rare:48 | ||||
| chrX:155026776-155027065 | Rare:79 |