| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33401481-33401609 | Rare:32 | ||||
| chr20:34303262-34303337 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:34677074-34677320 | Rare:64 | ||||
| chr20:35092765-35092948 | Common:2; Rare:86 | ||||
| chr20:35147271-35147423 | Common:1; Rare:50 | ||||
| chr20:35455046-35455206 | Common:1; Rare:54 | ||||
| chr20:35616905-35617033 | Common:1; Rare:26 | ||||
| chr20:35664880-35665004 | Common:1; Rare:33 | ||||
| chr20:35699186-35699279 | Rare:14 | ||||
| chr20:35699298-35699631 | Rare:102; Clinvar (benign):3 | ||||
| chr20:35742175-35742651 | Common:5; Rare:153 | ||||
| chr20:35771790-35772044 | Common:2; Rare:78 | ||||
| chr20:36461133-36461486 | Common:1; Rare:102 | ||||
| chr20:36605496-36605805 | Common:2; Rare:112 | ||||
| chr20:36746065-36746151 | Common:2; Rare:45 |