| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103214945-103215231 | Common:2; Rare:56 | ||||
| chrX:103255072-103255217 | Rare:16 | ||||
| chrX:103356385-103356727 | Common:3; Rare:48 | ||||
| chrX:103376391-103376613 | Common:1; Rare:34 | ||||
| chrX:103585445-103585696 | Common:3; Rare:50 | ||||
| chrX:103628892-103628998 | Rare:13 | ||||
| chrX:103629435-103629527 | Common:1; Rare:27 | ||||
| chrX:103686648-103687046 | Common:4; Rare:56 | ||||
| chrX:103687071-103687292 | Rare:35 | ||||
| chrX:103776734-103776982 | Common:2; Rare:34; Clinvar (benign):1 | ||||
| chrX:103780839-103781161 | Common:1; Rare:46 | ||||
| chrX:103781168-103781336 | Rare:21 | ||||
| chrX:103919087-103919208 | Common:2; Rare:25 | ||||
| chrX:104156894-104157080 | Common:1; Rare:30 | ||||
| chrX:106611706-106612018 | Rare:64 |