| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:104166314-104166525 | Common:1; Rare:56 | ||||
| chrX:106802439-106802758 | Common:1; Rare:59 | ||||
| chrX:107118771-107118907 | Common:2; Rare:31 | ||||
| chrX:107628425-107628520 | Common:1; Rare:11; Clinvar (benign):1 | ||||
| chrX:107716399-107716635 | Common:1; Rare:30 | ||||
| chrX:108091492-108091819 | Rare:91 | ||||
| chrX:108439505-108439853 | Common:2; Rare:82 | ||||
| chrX:109733150-109733491 | Common:1; Rare:81 | ||||
| chrX:110318023-110318262 | Rare:60 | ||||
| chrX:111681061-111681302 | Rare:63; Clinvar (benign):7 | ||||
| chrX:111681552-111681705 | Rare:58 | ||||
| chrX:115561005-115561244 | Common:1; Rare:42 | ||||
| chrX:118345890-118346165 | Common:3; Rare:48 | ||||
| chrX:118346393-118346495 | Rare:23 | ||||
| chrX:119236551-119236687 | Rare:34 |