| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:67545497-67545752 | Rare:55; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:72938177-72938249 | |||||
| chrX:73944231-73944356 | Rare:29 | ||||
| chrX:74292497-74292743 | Rare:43 | ||||
| chrX:74420659-74420877 | Rare:65 | ||||
| chrX:107676972-107677129 | Rare:20 | ||||
| chrX:119606411-119606566 | Common:1; Rare:31 | ||||
| chrX:125204297-125204560 | Rare:29 | ||||
| chrX:125445601-125445795 | Common:2; Rare:36 | ||||
| chrX:134549639-134549808 | Common:1; Rare:38 | ||||
| chrX:135032980-135033044 | Rare:10 | ||||
| chrX:136909332-136909448 | Rare:29 | ||||
| chrX:154361308-154361749 | Common:1; Rare:85; Clinvar:9; Clinvar (benign):12 | ||||
| chrX:154367659-154368091 | Common:2; Rare:67; Clinvar:5; Clinvar (benign):9 | ||||
| chrY:3002784-3002920 | Rare:1 |