| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48911633-48911715 | Rare:21; Clinvar (benign):3 | ||||
| chrX:48911904-48912177 | Common:1; Rare:52 | ||||
| chrX:48919013-48919258 | Rare:40 | ||||
| chrX:48958317-48958451 | Rare:40 | ||||
| chrX:49002196-49002264 | Rare:23 | ||||
| chrX:49038045-49038285 | Rare:44 | ||||
| chrX:49079755-49079960 | Rare:25 | ||||
| chrX:49186276-49186466 | Common:1; Rare:33 | ||||
| chrX:49235462-49235551 | Common:1; Rare:7 | ||||
| chrX:50067513-50067619 | Rare:16; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:53082123-53082368 | Common:1; Rare:59 | ||||
| chrX:53225125-53225495 | Common:3; Rare:115 | ||||
| chrX:53382378-53382523 | Rare:33 | ||||
| chrX:53422616-53422732 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chrX:53434317-53434670 | Common:2; Rare:69 |