| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133356485-133356630 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr9:133375965-133376377 | Common:4; Rare:150 | ||||
| chr9:136410372-136410695 | Common:7; Rare:142 | ||||
| chr9:136849569-136849868 | Common:1; Rare:107 | ||||
| chr9:137188525-137188760 | Common:2; Rare:116 | ||||
| chr9:137205419-137205758 | Common:1; Rare:127 | ||||
| chr9:137578837-137579009 | Common:2; Rare:59 | ||||
| chr9:137618803-137619031 | Common:1; Rare:102 | ||||
| chrM:3168-3276 | |||||
| chrM:5577-5590 | |||||
| chrM:6358-7266 | |||||
| chrM:7441-7587 | |||||
| chrM:10393-10490 | |||||
| chrM:11172-11481 | |||||
| chrX:1392047-1392363 | Common:6; Rare:139 |