| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961264-123961433 | Common:2; Rare:22 | ||||
| chrX:123961480-123961850 | Rare:51 | ||||
| chrX:129906073-129906201 | Rare:31 | ||||
| chrX:130165688-130165908 | Rare:44; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132218068-132218287 | Rare:25 | ||||
| chrX:132489026-132489091 | Rare:10 | ||||
| chrX:135344595-135344823 | Common:2; Rare:42 | ||||
| chrX:135973683-135973835 | Rare:56 | ||||
| chrX:135985372-135985503 | Rare:38; Clinvar (benign):4 | ||||
| chrX:136767170-136767298 | Rare:22 | ||||
| chrX:139204974-139205183 | Common:1; Rare:34 | ||||
| chrX:139222857-139223090 | Rare:25 | ||||
| chrX:141177076-141177302 | Common:1; Rare:28 | ||||
| chrX:149540909-149541115 | Common:3; Rare:36 | ||||
| chrX:149938440-149938665 | Common:2; Rare:57 |