| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:15937-16428 | |||||
| chrX:1348801-1349012 | Common:4; Rare:67 | ||||
| chrX:1359850-1360098 | Common:6; Rare:52 | ||||
| chrX:1398570-1398771 | Common:6; Rare:56 | ||||
| chrX:1402062-1402105 | Common:1; Rare:16 | ||||
| chrX:2609154-2609436 | Common:1; Rare:91 | ||||
| chrX:7147171-7147288 | Rare:23 | ||||
| chrX:11351665-11351820 | Common:1; Rare:20 | ||||
| chrX:13762260-13762441 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:15298268-15298433 | Rare:17 | ||||
| chrX:15674682-15675009 | Common:4; Rare:62 | ||||
| chrX:15675173-15675478 | Common:7; Rare:51 | ||||
| chrX:15675606-15675744 | Common:1; Rare:31 | ||||
| chrX:16820083-16820246 | Rare:20 | ||||
| chrX:18886826-18887029 | Rare:30 |