| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137086955-137087108 | Rare:67; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137188547-137188717 | Common:2; Rare:85 | ||||
| chr9:137205596-137205719 | Rare:46 | ||||
| chr9:137578828-137578993 | Common:2; Rare:55 | ||||
| chr9:137618851-137619024 | Common:1; Rare:69 | ||||
| chrM:3209-3330 | |||||
| chrM:4048-4144 | |||||
| chrM:4855-5081 | |||||
| chrM:5147-5579 | |||||
| chrM:5584-5837 | |||||
| chrM:5839-6022 | |||||
| chrM:6187-6484 | |||||
| chrM:7103-7294 | |||||
| chrM:7879-8391 | |||||
| chrM:8406-8857 |