| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137129708-137129835 | Common:2; Rare:43 | ||||
| chr9:137217366-137217560 | Common:1; Rare:70 | ||||
| chr9:137223387-137223725 | Common:3; Rare:123 | ||||
| chr9:137490733-137490973 | Rare:29 | ||||
| chr9:137664694-137664934 | Common:2; Rare:51 | ||||
| chr9:137776400-137776636 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr9:137810226-137810252 | Rare:9 | ||||
| chr9:137811356-137811511 | Rare:33; Clinvar:2 | ||||
| chr9:137831031-137831152 | Rare:18 | ||||
| chr9:137831847-137831860 | Rare:1 | ||||
| chr9:137876680-137876790 | Common:2; Rare:13 | ||||
| chr9:137959978-137960289 | Common:13; Rare:78 | ||||
| chr9:138220930-138221193 | Common:1; Rare:75 | ||||
| chrM:15832-16426 | |||||
| chrX:685242-685360 | Common:3; Rare:34 |