| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:100820220-100820411 | Common:2; Rare:45 | ||||
| chrX:101407806-101408292 | Common:5; Rare:88; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:103214993-103215158 | Common:2; Rare:37 | ||||
| chrX:103629437-103629536 | Common:1; Rare:27 | ||||
| chrX:103686635-103686906 | Common:1; Rare:43 | ||||
| chrX:103919053-103919155 | Common:3; Rare:24 | ||||
| chrX:104156882-104157070 | Common:1; Rare:29 | ||||
| chrX:105822633-105822814 | Rare:23 | ||||
| chrX:107716292-107716711 | Common:1; Rare:62 | ||||
| chrX:107716807-107717192 | Common:2; Rare:54 | ||||
| chrX:107775610-107775907 | Rare:50 | ||||
| chrX:107775938-107776116 | Common:4; Rare:31 | ||||
| chrX:108091499-108091822 | Rare:87 | ||||
| chrX:108439479-108439878 | Common:2; Rare:90 | ||||
| chrX:109537065-109537239 | Common:1; Rare:36 |