| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159615404-159615701 | Common:2; Rare:90 | ||||
| chr2:159616418-159616549 | Common:1; Rare:28 | ||||
| chr2:159711983-159712294 | Common:3; Rare:87 | ||||
| chr2:159712372-159712606 | Common:2; Rare:90 | ||||
| chr2:160062482-160062722 | Common:5; Rare:60 | ||||
| chr2:160200203-160200371 | Rare:20 | ||||
| chr2:161160859-161161121 | Common:1; Rare:56 | ||||
| chr2:161308394-161308566 | Common:2; Rare:40 | ||||
| chr2:164841820-164841936 | Common:1; Rare:38 | ||||
| chr2:165469540-165469711 | Rare:29 | ||||
| chr2:165794155-165794307 | Common:2; Rare:46; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:169584242-169584424 | Rare:72 | ||||
| chr2:169584709-169584816 | Rare:29 | ||||
| chr2:169694334-169694469 | Common:2; Rare:52 | ||||
| chr2:170928917-170929349 | Common:4; Rare:127 |