| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63653407-63653641 | Common:2; Rare:28 | ||||
| chr20:63658240-63658364 | Common:3; Rare:41 | ||||
| chr20:63707850-63708118 | Rare:78 | ||||
| chr20:63865082-63865368 | Common:2; Rare:112 | ||||
| chr20:63969847-63970091 | Common:3; Rare:86 | ||||
| chr20:64079924-64080099 | Common:1; Rare:74 | ||||
| chr21:14383120-14383479 | Common:2; Rare:99 | ||||
| chr21:15064827-15065162 | Rare:107 | ||||
| chr21:17612719-17613082 | Common:1; Rare:146 | ||||
| chr21:17819327-17819421 | Common:1; Rare:34 | ||||
| chr21:25607467-25607593 | Rare:59 | ||||
| chr21:25734852-25735504 | Common:5; Rare:223 | ||||
| chr21:25735584-25735931 | Common:4; Rare:92 | ||||
| chr21:26170565-26170890 | Common:3; Rare:107; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26573112-26573190 | Rare:29 |