| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240025289-240025428 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136268-240136348 | Rare:34 | ||||
| chr2:241102276-241102399 | Common:2; Rare:41 | ||||
| chr2:241149450-241149619 | Common:2; Rare:52 | ||||
| chr2:241315156-241315296 | Common:1; Rare:48 | ||||
| chr2:241315653-241316007 | Common:5; Rare:135 | ||||
| chr2:241508551-241508872 | Common:1; Rare:102 | ||||
| chr2:241637527-241637704 | Common:1; Rare:96 | ||||
| chr2:241686785-241686946 | Rare:50 | ||||
| chr20:1118448-1118648 | Common:2; Rare:62 | ||||
| chr20:1325260-1325426 | Rare:40 | ||||
| chr20:1393005-1393215 | Common:1; Rare:90 | ||||
| chr20:2470706-2470997 | Common:4; Rare:99 | ||||
| chr20:2652438-2652649 | Common:7; Rare:71 | ||||
| chr20:2664171-2664265 | Common:2; Rare:41 |