| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58622790-58622985 | Common:1; Rare:41 | ||||
| chr21:16194263-16194568 | Common:2; Rare:85 | ||||
| chr21:45982506-45982763 | Rare:75; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr21:45991983-45992217 | Common:2; Rare:91; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr21:46124648-46124920 | Common:5; Rare:129; Clinvar:8; Clinvar (benign):7 | ||||
| chr21:46129763-46130057 | Common:3; Rare:112 | ||||
| chr22:22297926-22298196 | Common:13; Rare:108 | ||||
| chr22:30969058-30969283 | Common:2; Rare:64 | ||||
| chr22:37805619-37805721 | Rare:26 | ||||
| chr22:45891425-45891636 | Common:2; Rare:48 | ||||
| chr22:50545622-50545896 | Common:3; Rare:51 | ||||
| chr3:8515488-8515560 | Common:1; Rare:16 | ||||
| chr3:8548831-8549005 | Rare:43 | ||||
| chr3:40453163-40453417 | Common:6; Rare:56 | ||||
| chr3:56296449-56296648 | Common:1; Rare:49 |