| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:17878478-17878754 | Common:18; Rare:220 | ||||
| chr2:17879110-17879472 | Common:1; Rare:183 | ||||
| chr2:18560100-18560395 | Common:2; Rare:146 | ||||
| chr2:18560414-18561019 | Common:1; Rare:385 | ||||
| chr2:19901513-19901817 | Common:6; Rare:305 | ||||
| chr2:19901855-19902352 | Common:11; Rare:282 | ||||
| chr2:19990016-19990326 | Rare:186 | ||||
| chr2:20012639-20012836 | Common:9; Rare:117; Clinvar (benign):3 | ||||
| chr2:20051481-20051921 | Common:4; Rare:317 | ||||
| chr2:20051985-20052237 | Common:4; Rare:144 | ||||
| chr2:20223354-20223586 | Rare:71 | ||||
| chr2:20223980-20224154 | Common:1; Rare:33 | ||||
| chr2:20224938-20225315 | Common:3; Rare:251 | ||||
| chr2:20225349-20225671 | Common:2; Rare:175 | ||||
| chr2:20350311-20350495 | Common:1; Rare:137 |