| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63956359-63956665 | Common:1; Rare:119 | ||||
| chr20:63969842-63970111 | Common:3; Rare:93 | ||||
| chr20:63980971-63981249 | Common:4; Rare:91; Clinvar:7; Clinvar (benign):4 | ||||
| chr20:64079917-64080082 | Common:1; Rare:70 | ||||
| chr20:64164415-64164458 | Rare:5 | ||||
| chr21:14383082-14383486 | Common:2; Rare:115 | ||||
| chr21:17612816-17613056 | Common:1; Rare:108 | ||||
| chr21:17819327-17819414 | Rare:34 | ||||
| chr21:17819654-17819911 | Rare:60 | ||||
| chr21:20998190-20998514 | Rare:159 | ||||
| chr21:25607476-25607622 | Rare:68 | ||||
| chr21:25639690-25639829 | Common:1; Rare:36 | ||||
| chr21:25734855-25735478 | Common:5; Rare:215 | ||||
| chr21:26170572-26170926 | Common:5; Rare:114; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26171074-26171183 | Rare:32 |