| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61853960-61854108 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61854468-61854907 | Common:1; Rare:88 | ||||
| chr2:61888332-61888454 | Rare:60 | ||||
| chr2:61888473-61888994 | Common:3; Rare:192 | ||||
| chr2:61905524-61905898 | Common:1; Rare:130 | ||||
| chr2:62195558-62195710 | Common:1; Rare:24 | ||||
| chr2:62195861-62196214 | Common:3; Rare:117 | ||||
| chr2:62196365-62196539 | Rare:46 | ||||
| chr2:62505770-62506105 | Common:4; Rare:125 | ||||
| chr2:62506245-62506355 | Common:1; Rare:38 | ||||
| chr2:62506500-62506525 | Rare:6 | ||||
| chr2:62506529-62506557 | Common:1; Rare:5 | ||||
| chr2:62705123-62705767 | Common:2; Rare:169 | ||||
| chr2:62705917-62705970 | Rare:15 | ||||
| chr2:62706106-62706247 | Rare:39 |