| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62937875-62938193 | Common:2; Rare:117 | ||||
| chr20:63272687-63272863 | Common:5; Rare:59 | ||||
| chr20:63658233-63658380 | Common:4; Rare:52 | ||||
| chr20:63707865-63708118 | Rare:72 | ||||
| chr20:63740954-63741157 | Common:1; Rare:52 | ||||
| chr20:63865061-63865346 | Common:2; Rare:106 | ||||
| chr20:63969837-63970040 | Common:3; Rare:70 | ||||
| chr21:14383111-14383510 | Common:3; Rare:113 | ||||
| chr21:17512783-17513132 | Common:2; Rare:112 | ||||
| chr21:17819324-17819521 | Common:1; Rare:72 | ||||
| chr21:17819664-17819837 | Rare:41 | ||||
| chr21:25607471-25607622 | Rare:72 | ||||
| chr21:25734853-25735478 | Common:5; Rare:216 | ||||
| chr21:25735522-25735978 | Common:4; Rare:115 | ||||
| chr21:26170565-26170933 | Common:6; Rare:119; Clinvar:5; Clinvar (benign):2 |