| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120629927-120630266 | Common:4; Rare:65 | ||||
| chrX:123733025-123733152 | Rare:20 | ||||
| chrX:123961264-123961328 | Common:2; Rare:17 | ||||
| chrX:123961635-123961828 | Rare:28 | ||||
| chrX:129779808-129779975 | Rare:26 | ||||
| chrX:129906046-129906195 | Rare:41 | ||||
| chrX:130165657-130165983 | Rare:71; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171831-130171996 | Common:1; Rare:41 | ||||
| chrX:130401908-130402017 | Common:2; Rare:32 | ||||
| chrX:132023144-132023316 | Rare:44 | ||||
| chrX:135973720-135973870 | Rare:48 | ||||
| chrX:149505226-149505415 | Rare:61 | ||||
| chrX:149540827-149541054 | Common:4; Rare:41 | ||||
| chrX:149938440-149938593 | Common:1; Rare:42 | ||||
| chrX:151397030-151397295 | Common:5; Rare:130 |