| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:81201941-81202139 | Rare:37 | ||||
| chrX:101407923-101408257 | Common:3; Rare:53; Clinvar (benign):5 | ||||
| chrX:103356366-103356564 | Common:3; Rare:31 | ||||
| chrX:104156967-104157066 | Common:1; Rare:17 | ||||
| chrX:108091462-108091788 | Rare:85 | ||||
| chrX:119871702-119871904 | Common:1; Rare:51; Clinvar (benign):2 | ||||
| chrX:120560465-120560798 | Rare:55; Clinvar:2 | ||||
| chrX:130110489-130110677 | Common:1; Rare:39 | ||||
| chrX:135344712-135344816 | Rare:19 | ||||
| chrX:152830718-152831099 | Common:2; Rare:65 | ||||
| chrX:153794324-153794672 | Common:1; Rare:110; Clinvar (benign):2 | ||||
| chrX:153797529-153797810 | Common:2; Rare:90 | ||||
| chrX:153934977-153935041 | Rare:19 | ||||
| chrX:154428472-154428728 | Common:2; Rare:48 | ||||
| chrX:154547550-154547662 | Common:1; Rare:29; Clinvar (benign):1 |