| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:100820203-100820443 | Common:2; Rare:57 | ||||
| chrX:101407897-101408282 | Common:5; Rare:69; Clinvar (benign):9 | ||||
| chrX:102142399-102142593 | Rare:49 | ||||
| chrX:102651318-102651489 | Common:2; Rare:52 | ||||
| chrX:102712795-102712894 | Rare:13 | ||||
| chrX:103376397-103376607 | Common:1; Rare:34 | ||||
| chrX:103585445-103585682 | Common:3; Rare:47 | ||||
| chrX:103586437-103586849 | Rare:88 | ||||
| chrX:103607759-103608037 | Common:1; Rare:47 | ||||
| chrX:103686643-103686872 | Common:1; Rare:37 | ||||
| chrX:103686989-103687283 | Rare:46 | ||||
| chrX:103710612-103710910 | Common:2; Rare:32 | ||||
| chrX:103776651-103776918 | Common:2; Rare:24 | ||||
| chrX:104156902-104157052 | Common:1; Rare:25 | ||||
| chrX:104254865-104255115 | Common:1; Rare:58 |