| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35147121-35147184 | Rare:20 | ||||
| chr20:35147255-35147373 | Common:1; Rare:45 | ||||
| chr20:35172032-35172114 | Rare:15 | ||||
| chr20:35172143-35172184 | Rare:12 | ||||
| chr20:35284728-35284880 | Common:1; Rare:53 | ||||
| chr20:35542322-35542552 | Rare:78 | ||||
| chr20:35556969-35557272 | Common:2; Rare:95 | ||||
| chr20:35664880-35665015 | Common:1; Rare:34 | ||||
| chr20:35699292-35699456 | Rare:55; Clinvar (benign):3 | ||||
| chr20:35705236-35705412 | Rare:38 | ||||
| chr20:35740822-35741152 | Common:3; Rare:88 | ||||
| chr20:35742068-35742601 | Common:5; Rare:163 | ||||
| chr20:35771684-35772044 | Common:2; Rare:102 | ||||
| chr20:36746062-36746311 | Common:2; Rare:88 | ||||
| chr20:36875993-36876197 | Rare:53 |