| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62937381-62937535 | Common:2; Rare:48 | ||||
| chr20:62937893-62938180 | Common:2; Rare:101 | ||||
| chr20:62952583-62953083 | Common:7; Rare:151; Clinvar (pathogenic):1 | ||||
| chr20:63272726-63272886 | Common:1; Rare:56 | ||||
| chr20:63658225-63658364 | Common:4; Rare:46 | ||||
| chr20:63707283-63707416 | Rare:44 | ||||
| chr20:63707875-63708098 | Rare:63 | ||||
| chr20:63865079-63865351 | Common:2; Rare:106 | ||||
| chr20:64079918-64080082 | Common:1; Rare:70 | ||||
| chr21:17819332-17819488 | Common:1; Rare:54 | ||||
| chr21:25607462-25607612 | Rare:72 | ||||
| chr21:25734855-25734983 | Common:2; Rare:58 | ||||
| chr21:25735009-25735444 | Common:1; Rare:133 | ||||
| chr21:25735597-25735850 | Common:3; Rare:61 | ||||
| chr21:26170666-26170895 | Common:3; Rare:77; Clinvar:4; Clinvar (benign):2 |