| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:12562-13279 | |||||
| chrM:13285-14223 | |||||
| chrM:14273-14825 | |||||
| chrM:14945-15895 | |||||
| chrX:276206-276383 | Common:3; Rare:57 | ||||
| chrX:281307-281410 | Common:1; Rare:25 | ||||
| chrX:1392044-1392383 | Common:6; Rare:150 | ||||
| chrX:1537115-1537289 | Rare:38 | ||||
| chrX:1591508-1591669 | Rare:77 | ||||
| chrX:2691185-2691356 | Common:7; Rare:68 | ||||
| chrX:2929252-2929420 | Common:2; Rare:43 | ||||
| chrX:7927347-7927530 | Common:1; Rare:44 | ||||
| chrX:12791310-12791416 | Rare:15 | ||||
| chrX:13734543-13734852 | Common:3; Rare:93; Clinvar (benign):1 | ||||
| chrX:14029838-14030016 | Common:2; Rare:54 |