| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107628316-107628517 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chrX:107715987-107716302 | Rare:50 | ||||
| chrX:107716392-107716849 | Common:1; Rare:79 | ||||
| chrX:107716917-107717193 | Common:2; Rare:33 | ||||
| chrX:107775742-107775907 | Rare:33 | ||||
| chrX:108091516-108091818 | Rare:80 | ||||
| chrX:108439457-108439882 | Common:3; Rare:96 | ||||
| chrX:109733171-109733500 | Common:1; Rare:78 | ||||
| chrX:110318051-110318271 | Rare:54 | ||||
| chrX:115560987-115561244 | Common:1; Rare:47 | ||||
| chrX:118345904-118346137 | Common:2; Rare:42 | ||||
| chrX:119468215-119468612 | Common:3; Rare:113 | ||||
| chrX:119574374-119574581 | Rare:47 | ||||
| chrX:119791572-119791978 | Common:2; Rare:108 | ||||
| chrX:119852921-119853276 | Common:3; Rare:58; Clinvar (benign):3 |