| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119468180-119468610 | Common:4; Rare:120 | ||||
| chrX:119469051-119469209 | Rare:45 | ||||
| chrX:119469546-119469750 | Common:3; Rare:35 | ||||
| chrX:119574322-119574924 | Common:3; Rare:175 | ||||
| chrX:119606351-119606602 | Common:1; Rare:89 | ||||
| chrX:119693100-119693324 | Rare:88 | ||||
| chrX:119791562-119791995 | Common:2; Rare:167 | ||||
| chrX:119852510-119852850 | Rare:105 | ||||
| chrX:119852918-119853289 | Common:6; Rare:117; Clinvar (benign):6 | ||||
| chrX:119871662-119871970 | Common:2; Rare:121; Clinvar (benign):6 | ||||
| chrX:119943594-119943862 | Rare:89 | ||||
| chrX:120250556-120250872 | Common:4; Rare:48 | ||||
| chrX:120469152-120469483 | Common:1; Rare:62; Clinvar:7; Clinvar (benign):4 | ||||
| chrX:120559860-120560210 | Rare:81 | ||||
| chrX:120560510-120560880 | Rare:75; Clinvar:1 |