| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:265195-265239 | Common:1; Rare:13 | ||||
| chr2:676306-676420 | Common:1; Rare:26 | ||||
| chr2:676658-677246 | Common:5; Rare:166 | ||||
| chr2:677252-677774 | Common:4; Rare:188 | ||||
| chr2:1744476-1744638 | Common:1; Rare:54 | ||||
| chr2:3377359-3377452 | Common:1; Rare:14 | ||||
| chr2:3377638-3378146 | Common:2; Rare:156 | ||||
| chr2:3379511-3379861 | Common:3; Rare:125 | ||||
| chr2:3379900-3380019 | Common:1; Rare:27 | ||||
| chr2:3380096-3380176 | Rare:16 | ||||
| chr2:3518766-3519376 | Common:5; Rare:187 | ||||
| chr2:3519476-3519736 | Common:3; Rare:76 | ||||
| chr2:3558210-3558763 | Common:6; Rare:194 | ||||
| chr2:3575057-3575392 | Common:3; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3605221-3605581 | Common:7; Rare:40 |