| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:294-1017 | |||||
| chrM:1667-1765 | |||||
| chrM:6520-6731 | |||||
| chrM:6897-6976 | |||||
| chrM:16326-16397 | |||||
| chrX:1359841-1360091 | Common:6; Rare:55 | ||||
| chrX:1360353-1360617 | Common:3; Rare:72 | ||||
| chrX:1361258-1361348 | Common:2; Rare:26 | ||||
| chrX:1362639-1362736 | Common:1; Rare:29 | ||||
| chrX:1571070-1571269 | Common:4; Rare:41 | ||||
| chrX:2609154-2609407 | Rare:80 | ||||
| chrX:2740678-2740803 | Common:2; Rare:28; Clinvar:1 | ||||
| chrX:3814787-3815106 | Common:3; Rare:78 | ||||
| chrX:15675617-15675720 | Rare:19 | ||||
| chrX:20176296-20176452 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 |