| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133356466-133356608 | Common:1; Rare:64; Clinvar (benign):2 | ||||
| chr9:133375973-133376366 | Common:3; Rare:143 | ||||
| chr9:136410411-136410671 | Common:6; Rare:112 | ||||
| chr9:137188547-137188723 | Common:2; Rare:90 | ||||
| chr9:137618789-137619043 | Common:1; Rare:116 | ||||
| chrM:5436-5610 | |||||
| chrM:6361-7315 | |||||
| chrM:7381-7603 | |||||
| chrM:7777-8152 | |||||
| chrM:8262-8395 | |||||
| chrM:9161-9438 | |||||
| chrM:10185-10521 | |||||
| chrX:276248-276375 | Common:3; Rare:43 | ||||
| chrX:11111141-11111344 | Common:3; Rare:40 | ||||
| chrX:12975005-12975137 | Common:1; Rare:30 |