| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:83507971-83508331 | Common:2; Rare:82 | ||||
| chrX:85243715-85244178 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chrX:86047494-86047659 | Common:1; Rare:37 | ||||
| chrX:91434726-91434848 | Rare:23 | ||||
| chrX:93673493-93673744 | Common:1; Rare:41 | ||||
| chrX:93673950-93674180 | Rare:29 | ||||
| chrX:96684358-96684866 | Common:1; Rare:83 | ||||
| chrX:100410255-100410430 | Common:2; Rare:40 | ||||
| chrX:101052071-101052203 | Rare:19 | ||||
| chrX:101390781-101391050 | Rare:72 | ||||
| chrX:101407897-101408307 | Common:5; Rare:75; Clinvar (benign):9 | ||||
| chrX:101418223-101418287 | Common:1; Rare:8 | ||||
| chrX:101485250-101485503 | Rare:40 | ||||
| chrX:101550147-101550453 | Common:1; Rare:36 | ||||
| chrX:101623031-101623215 | Rare:36 |