| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215311895-215312152 | Common:8; Rare:106 | ||||
| chr2:215349048-215349471 | Common:1; Rare:141 | ||||
| chr2:215366062-215366101 | Rare:7 | ||||
| chr2:215369836-215370125 | Common:4; Rare:46 | ||||
| chr2:215409984-215410227 | Rare:51 | ||||
| chr2:215435693-215435780 | Common:2; Rare:21 | ||||
| chr2:215435852-215436284 | Common:2; Rare:118 | ||||
| chr2:216081743-216081932 | Common:1; Rare:65 | ||||
| chr2:216372117-216372584 | Rare:95 | ||||
| chr2:216412694-216412786 | Rare:11 | ||||
| chr2:216498685-216498917 | Common:8; Rare:102 | ||||
| chr2:216633783-216633969 | Rare:41 | ||||
| chr2:216695345-216695699 | Rare:68 | ||||
| chr2:218217003-218217391 | Common:3; Rare:122 | ||||
| chr2:218270091-218270562 | Common:5; Rare:149; Clinvar:4; Clinvar (benign):2 |