| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35096525-35096789 | Common:1; Rare:63 | ||||
| chr9:35102806-35102933 | Rare:32 | ||||
| chr9:35103078-35103178 | Common:1; Rare:43 | ||||
| chr9:35103182-35103214 | Rare:4 | ||||
| chr9:35103430-35103646 | Rare:41 | ||||
| chr9:35161819-35162149 | Common:4; Rare:94 | ||||
| chr9:35162277-35162300 | Rare:8 | ||||
| chr9:35489793-35490144 | Common:3; Rare:111 | ||||
| chr9:35490325-35490569 | Rare:51 | ||||
| chr9:35657841-35658455 | Common:11; Rare:478; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35665197-35665324 | Common:2; Rare:45 | ||||
| chr9:35675849-35676008 | Common:3; Rare:66 | ||||
| chr9:35689144-35689435 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:35689777-35690102 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35691063-35691397 | Common:1; Rare:70 |