| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15510867-15511023 | Rare:68 | ||||
| chr9:15552650-15553280 | Common:7; Rare:395 | ||||
| chr9:17134859-17135066 | Rare:163 | ||||
| chr9:19049143-19049504 | Common:1; Rare:217 | ||||
| chr9:19102850-19103084 | Common:3; Rare:164 | ||||
| chr9:19127402-19127762 | Common:9; Rare:158 | ||||
| chr9:19230215-19230519 | Common:8; Rare:205 | ||||
| chr9:19230633-19230882 | Common:6; Rare:214 | ||||
| chr9:19380157-19380403 | Common:11; Rare:219 | ||||
| chr9:19408772-19409014 | Common:4; Rare:94 | ||||
| chr9:20684000-20684296 | Common:7; Rare:177 | ||||
| chr9:21335321-21335491 | Common:6; Rare:111 | ||||
| chr9:21802508-21802735 | Common:1; Rare:116; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:21974451-21974980 | Common:4; Rare:299; Clinvar:75; Clinvar (benign):54; Clinvar (pathogenic):7 | ||||
| chr9:21994300-21994810 | Common:4; Rare:270; Clinvar:5; Clinvar (benign):9 |