| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74454760-74455164 | Rare:516 | ||||
| chr2:74458064-74458471 | Common:3; Rare:348 | ||||
| chr2:74459104-74459504 | Common:1; Rare:67 | ||||
| chr2:74464515-74464915 | Rare:131; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:74465012-74465570 | Common:10; Rare:393; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr2:74471951-74472482 | Common:2; Rare:417 | ||||
| chr2:74472389-74473156 | Common:27; Rare:1591 | ||||
| chr2:74482116-74482780 | Common:1; Rare:312 | ||||
| chr2:74482705-74483122 | Common:5; Rare:480 | ||||
| chr2:74483095-74483530 | Common:14; Rare:807 | ||||
| chr2:74502340-74502687 | Common:1; Rare:191 | ||||
| chr2:74502648-74503230 | Common:6; Rare:350 | ||||
| chr2:74503140-74503786 | Common:3; Rare:502 | ||||
| chr2:74506653-74506806 | Common:2; Rare:49 | ||||
| chr2:74506712-74507112 | Common:2; Rare:106 |