| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62926457-62926635 | Common:2; Rare:57 | ||||
| chr20:62937887-62938165 | Common:1; Rare:99 | ||||
| chr20:63658244-63658356 | Common:2; Rare:36 | ||||
| chr20:63707283-63707449 | Rare:51 | ||||
| chr20:63707875-63708109 | Rare:69 | ||||
| chr20:63864941-63865345 | Common:2; Rare:144 | ||||
| chr21:25734863-25734972 | Common:2; Rare:47 | ||||
| chr21:25734996-25735066 | Rare:27 | ||||
| chr21:25735272-25735421 | Common:1; Rare:36 | ||||
| chr21:25735595-25735824 | Common:3; Rare:57 | ||||
| chr21:26170676-26170883 | Common:3; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
| chr21:29024534-29024716 | Common:2; Rare:79 | ||||
| chr21:29073562-29073872 | Common:2; Rare:97 | ||||
| chr21:29298716-29298957 | Common:2; Rare:102 | ||||
| chr21:31659502-31659837 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 |