| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25696800-25696905 | Common:1; Rare:31 | ||||
| chr20:31547272-31547432 | Rare:39 | ||||
| chr20:31739107-31739362 | Common:1; Rare:64 | ||||
| chr20:32207686-32207934 | Common:3; Rare:93 | ||||
| chr20:33401482-33401589 | Rare:29 | ||||
| chr20:34112195-34112423 | Rare:65 | ||||
| chr20:34516312-34516446 | Common:3; Rare:49 | ||||
| chr20:34677089-34677320 | Rare:58 | ||||
| chr20:35092787-35092948 | Common:1; Rare:72 | ||||
| chr20:35284716-35284870 | Common:1; Rare:52 | ||||
| chr20:35542343-35542487 | Rare:47 | ||||
| chr20:35699295-35699475 | Rare:63; Clinvar (benign):3 | ||||
| chr20:35742182-35742584 | Common:4; Rare:123 | ||||
| chr20:36461160-36461470 | Common:1; Rare:87 | ||||
| chr20:37095953-37096269 | Common:1; Rare:101 |