| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103629441-103629536 | Rare:27 | ||||
| chrX:103688004-103688403 | Common:1; Rare:48 | ||||
| chrX:103776630-103776874 | Common:2; Rare:25 | ||||
| chrX:103919037-103919178 | Common:4; Rare:30 | ||||
| chrX:104156891-104157063 | Common:1; Rare:28 | ||||
| chrX:107628269-107628519 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chrX:107716223-107716690 | Common:1; Rare:75 | ||||
| chrX:107716917-107717197 | Common:2; Rare:34 | ||||
| chrX:108091520-108091818 | Rare:80 | ||||
| chrX:109733127-109733562 | Common:1; Rare:98 | ||||
| chrX:110318070-110318251 | Rare:47 | ||||
| chrX:111680970-111681336 | Rare:91; Clinvar (benign):7 | ||||
| chrX:115593483-115593606 | Common:1; Rare:17 | ||||
| chrX:118976077-118976108 | Rare:6 | ||||
| chrX:119236566-119236651 | Rare:23 |