| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:12896-13057 | |||||
| chrM:15809-16000 | |||||
| chrX:2609162-2609442 | Common:1; Rare:88 | ||||
| chrX:15675383-15675478 | Common:4; Rare:13 | ||||
| chrX:15675628-15675735 | Common:1; Rare:22 | ||||
| chrX:29660050-29660200 | Common:3; Rare:26 | ||||
| chrX:45770128-45770451 | Rare:28 | ||||
| chrX:45771234-45771464 | Rare:24 | ||||
| chrX:47199097-47199306 | Common:1; Rare:46; Clinvar (benign):4 | ||||
| chrX:100690156-100690180 | Common:1; Rare:2 | ||||
| chrX:154362298-154362533 | Common:1; Rare:70; Clinvar:7; Clinvar (benign):6 |