| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103919027-103919155 | Common:4; Rare:26 | ||||
| chrX:104156882-104157070 | Common:1; Rare:29 | ||||
| chrX:107118764-107118889 | Common:2; Rare:25 | ||||
| chrX:107628365-107628541 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:107716404-107717113 | Common:3; Rare:108 | ||||
| chrX:107775582-107775622 | Rare:2 | ||||
| chrX:107775634-107775983 | Common:1; Rare:60 | ||||
| chrX:107825471-107825755 | Common:2; Rare:26 | ||||
| chrX:107825827-107825904 | Rare:9 | ||||
| chrX:108091516-108091829 | Rare:83 | ||||
| chrX:108438222-108438539 | Rare:48 | ||||
| chrX:108439429-108440085 | Common:3; Rare:137 | ||||
| chrX:109733145-109733491 | Common:1; Rare:82 | ||||
| chrX:110795724-110795888 | Rare:18 | ||||
| chrX:111681552-111681757 | Rare:70 |