| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:165469513-165469703 | Rare:32 | ||||
| chr2:165572244-165572484 | Rare:36 | ||||
| chr2:165574115-165574408 | Rare:62 | ||||
| chr2:165953693-165954128 | Common:4; Rare:155; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:165954165-165954324 | Common:1; Rare:37 | ||||
| chr2:166375820-166376260 | Common:5; Rare:118; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:166494100-166494530 | Common:1; Rare:79 | ||||
| chr2:168247695-168247961 | Rare:86 | ||||
| chr2:168456118-168456295 | Rare:47 | ||||
| chr2:168456584-168456818 | Rare:77 | ||||
| chr2:168890363-168890604 | Common:2; Rare:55 | ||||
| chr2:169362495-169362727 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169478543-169478943 | Common:4; Rare:74 | ||||
| chr2:169479358-169479556 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr2:169479610-169479850 | Common:1; Rare:70 |