| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136981668-136981842 | Common:2; Rare:40 | ||||
| chr9:137086698-137087146 | Common:2; Rare:184; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188537-137188713 | Common:2; Rare:84 | ||||
| chr9:137205377-137205738 | Common:1; Rare:126 | ||||
| chr9:137423141-137423523 | Common:2; Rare:119 | ||||
| chr9:137454874-137455054 | Rare:34 | ||||
| chr9:137550379-137550483 | Rare:14 | ||||
| chr9:137551611-137551963 | Common:29; Rare:147 | ||||
| chr9:137578864-137579016 | Common:2; Rare:51 | ||||
| chr9:137618783-137619046 | Common:1; Rare:120 | ||||
| chrM:4312-4332 | |||||
| chrM:7368-7588 | |||||
| chrM:7605-8161 | |||||
| chrM:8531-9043 | |||||
| chrM:9142-9809 |