| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:9953-10176 | |||||
| chrM:10461-10786 | |||||
| chrM:13649-14605 | |||||
| chrX:276208-276375 | Common:3; Rare:55 | ||||
| chrX:1391924-1392406 | Common:6; Rare:214 | ||||
| chrX:2691177-2691520 | Common:9; Rare:161 | ||||
| chrX:7927370-7927512 | Common:1; Rare:35 | ||||
| chrX:7927697-7927799 | Rare:24 | ||||
| chrX:11111196-11111382 | Common:4; Rare:37 | ||||
| chrX:11665075-11665366 | Rare:47 | ||||
| chrX:11757900-11758266 | Common:2; Rare:70 | ||||
| chrX:12791301-12791439 | Rare:22 | ||||
| chrX:12975005-12975240 | Common:2; Rare:55 | ||||
| chrX:13734543-13734870 | Common:3; Rare:96; Clinvar (benign):1 | ||||
| chrX:14029792-14029980 | Common:1; Rare:60 |