| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:32550910-32551103 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:33036760-33037106 | Common:2; Rare:79 | ||||
| chr9:33165834-33166011 | Common:1; Rare:32 | ||||
| chr9:33251207-33251455 | Rare:36 | ||||
| chr9:33265772-33266112 | Rare:76 | ||||
| chr9:33752268-33752578 | Common:1; Rare:58 | ||||
| chr9:33916758-33917089 | Common:1; Rare:74 | ||||
| chr9:34224257-34224488 | Common:1; Rare:58 | ||||
| chr9:34241171-34241199 | Rare:7 | ||||
| chr9:35604026-35604196 | Common:3; Rare:44 | ||||
| chr9:35684247-35684556 | Rare:70; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:35706766-35707155 | Common:2; Rare:112 | ||||
| chr9:35724573-35724960 | Common:1; Rare:86 | ||||
| chr9:35740600-35740648 | Rare:19; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:35772061-35772241 | Rare:31 |