| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:153478775-153478947 | Common:1; Rare:51 | ||||
| chr2:158968487-158968678 | Rare:59 | ||||
| chr2:159286596-159286865 | Common:4; Rare:95 | ||||
| chr2:159615213-159615330 | Common:2; Rare:25 | ||||
| chr2:159616417-159616568 | Common:1; Rare:30 | ||||
| chr2:159711983-159712290 | Common:2; Rare:87 | ||||
| chr2:159712382-159712591 | Common:2; Rare:86 | ||||
| chr2:159904718-159904863 | Rare:31 | ||||
| chr2:162343893-162344202 | Common:1; Rare:100 | ||||
| chr2:165469569-165469711 | Rare:25 | ||||
| chr2:165794128-165794367 | Common:2; Rare:67; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165953748-165953807 | Rare:35; Clinvar:5 | ||||
| chr2:169584276-169584622 | Common:1; Rare:130 | ||||
| chr2:169584703-169584809 | Rare:27 | ||||
| chr2:169694376-169694493 | Common:2; Rare:33 |