| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24971902-24972153 | Common:1; Rare:81 | ||||
| chr2:25251529-25251721 | Rare:42 | ||||
| chr2:25252228-25252515 | Rare:64 | ||||
| chr2:25878446-25878772 | Common:4; Rare:99 | ||||
| chr2:26033764-26034159 | Common:4; Rare:148 | ||||
| chr2:26034320-26034513 | Common:1; Rare:49 | ||||
| chr2:26244564-26245037 | Common:2; Rare:165; Clinvar:7; Clinvar (benign):9 | ||||
| chr2:26345789-26346234 | Common:1; Rare:137 | ||||
| chr2:26764210-26764337 | Rare:52 | ||||
| chr2:27032822-27033018 | Rare:78 | ||||
| chr2:27051546-27051689 | Rare:43 | ||||
| chr2:27071543-27071909 | Common:1; Rare:108 | ||||
| chr2:27093963-27094162 | Common:1; Rare:41 | ||||
| chr2:27211730-27212088 | Common:3; Rare:122 | ||||
| chr2:27212215-27212398 | Common:2; Rare:101 |