| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:32550908-32551308 | Common:1; Rare:244; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:33030260-33030830 | Rare:138 | ||||
| chr9:33081300-33081630 | Common:2; Rare:138 | ||||
| chr9:33103760-33104370 | Common:8; Rare:187 | ||||
| chr9:33113240-33113846 | Common:6; Rare:291; Clinvar:9; Clinvar (benign):5 | ||||
| chr9:33161066-33161318 | Rare:77 | ||||
| chr9:33162807-33163110 | Common:2; Rare:117 | ||||
| chr9:33165460-33165792 | Rare:119 | ||||
| chr9:33165820-33166019 | Common:2; Rare:70 | ||||
| chr9:33185055-33185350 | Rare:94 | ||||
| chr9:33229773-33230028 | Rare:87 | ||||
| chr9:33231378-33231546 | Common:2; Rare:59 | ||||
| chr9:33232915-33233122 | Common:4; Rare:67 | ||||
| chr9:33234033-33234276 | Common:1; Rare:92 | ||||
| chr9:33234277-33234440 | Common:3; Rare:28 |