| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:21031446-21031710 | Common:3; Rare:108 | ||||
| chr9:21802534-21802745 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:26892731-26892887 | Common:1; Rare:77 | ||||
| chr9:26947024-26947273 | Common:1; Rare:95 | ||||
| chr9:26947402-26947571 | Common:1; Rare:55 | ||||
| chr9:26956275-26956459 | Common:2; Rare:72 | ||||
| chr9:27529744-27529762 | Rare:8 | ||||
| chr9:27529764-27529886 | Common:4; Rare:41 | ||||
| chr9:27573422-27573553 | Common:5; Rare:79 | ||||
| chr9:27573729-27573972 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:33001538-33001797 | Common:3; Rare:120; Clinvar (benign):4 | ||||
| chr9:33025071-33025355 | Common:7; Rare:120 | ||||
| chr9:33076583-33076865 | Common:2; Rare:91 | ||||
| chr9:33166837-33166963 | Rare:47; Clinvar:1 | ||||
| chr9:33264568-33264877 | Common:1; Rare:92 |