| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164621088-164621801 | Common:5; Rare:223 | ||||
| chr2:164694001-164694553 | Common:5; Rare:221 | ||||
| chr2:164840364-164840815 | Common:2; Rare:133 | ||||
| chr2:164841144-164841601 | Rare:250 | ||||
| chr2:164841738-164842236 | Common:6; Rare:238 | ||||
| chr2:164937830-164938304 | Common:4; Rare:135 | ||||
| chr2:165953703-165953956 | Common:4; Rare:186; Clinvar:15; Clinvar (benign):3 | ||||
| chr2:166375832-166376189 | Common:7; Rare:158; Clinvar:2; Clinvar (benign):10 | ||||
| chr2:168247433-168247743 | Common:10; Rare:242 | ||||
| chr2:168455565-168456096 | Common:14; Rare:187 | ||||
| chr2:168456112-168456367 | Rare:154 | ||||
| chr2:168456544-168456880 | Rare:195 | ||||
| chr2:169362491-169362628 | Common:1; Rare:22; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169479373-169479556 | Common:6; Rare:139; Clinvar (benign):2 | ||||
| chr2:169584277-169584674 | Common:2; Rare:281 |