| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34677069-34677304 | Rare:61 | ||||
| chr20:34955741-34955868 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35092765-35092965 | Common:2; Rare:87 | ||||
| chr20:35147306-35147407 | Rare:28 | ||||
| chr20:35284734-35284870 | Common:1; Rare:48 | ||||
| chr20:35455066-35455319 | Common:1; Rare:90 | ||||
| chr20:35556683-35557014 | Common:2; Rare:85 | ||||
| chr20:35664862-35664984 | Common:1; Rare:37 | ||||
| chr20:35699295-35699475 | Rare:63; Clinvar (benign):3 | ||||
| chr20:35742103-35742657 | Common:5; Rare:179 | ||||
| chr20:36236250-36236491 | Common:2; Rare:49 | ||||
| chr20:36461144-36461498 | Common:1; Rare:105 | ||||
| chr20:36573332-36573627 | Common:1; Rare:129 | ||||
| chr20:36574425-36574567 | Rare:60 | ||||
| chr20:37095946-37096269 | Common:1; Rare:103 |