| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:109733178-109733479 | Common:1; Rare:70 | ||||
| chrX:119236465-119236649 | Rare:55 | ||||
| chrX:119399018-119399362 | Common:3; Rare:65 | ||||
| chrX:119468215-119468501 | Common:3; Rare:97 | ||||
| chrX:119791624-119791971 | Common:2; Rare:83 | ||||
| chrX:119871648-119871916 | Common:1; Rare:57; Clinvar (benign):3 | ||||
| chrX:120469113-120469378 | Common:1; Rare:61; Clinvar:9; Clinvar (benign):5 | ||||
| chrX:120560438-120560861 | Rare:65; Clinvar:2 | ||||
| chrX:120603955-120604188 | Rare:41 | ||||
| chrX:123733022-123733177 | Rare:28 | ||||
| chrX:130110495-130110677 | Common:1; Rare:39 | ||||
| chrX:130165739-130165937 | Rare:34; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:136497359-136497620 | Common:1; Rare:62 | ||||
| chrX:149540435-149540719 | Common:1; Rare:34 | ||||
| chrX:149540721-149541034 | Common:4; Rare:61 |