| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237487090-237487323 | Common:3; Rare:66 | ||||
| chr2:237591359-237591516 | Common:3; Rare:41 | ||||
| chr2:237591559-237591860 | Common:2; Rare:76 | ||||
| chr2:237966719-237967123 | Common:4; Rare:123 | ||||
| chr2:237968650-237968812 | Common:2; Rare:30 | ||||
| chr2:238060687-238061158 | Common:7; Rare:151 | ||||
| chr2:238203583-238203821 | Common:3; Rare:101 | ||||
| chr2:238426892-238427058 | Common:1; Rare:61 | ||||
| chr2:239401641-239401798 | Rare:83 | ||||
| chr2:240025240-240025480 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136255-240136439 | Common:1; Rare:81 | ||||
| chr2:240560754-240560873 | Common:1; Rare:51 | ||||
| chr2:240561077-240561322 | Common:4; Rare:103 | ||||
| chr2:241102279-241102401 | Common:2; Rare:40 | ||||
| chr2:241149434-241149613 | Common:2; Rare:59 |