| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162343854-162344224 | Common:2; Rare:122 | ||||
| chr2:162344316-162344403 | Common:1; Rare:28 | ||||
| chr2:163735882-163736113 | Common:1; Rare:36 | ||||
| chr2:164841821-164841926 | Common:1; Rare:34 | ||||
| chr2:165093813-165093926 | Rare:14 | ||||
| chr2:165469536-165469711 | Rare:30 | ||||
| chr2:165794168-165794335 | Common:2; Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:165953683-165954041 | Common:2; Rare:143; Clinvar:11; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:166375867-166376290 | Common:5; Rare:112; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:168247683-168247970 | Common:1; Rare:91 | ||||
| chr2:168456105-168456437 | Rare:114 | ||||
| chr2:168456544-168456814 | Rare:91 | ||||
| chr2:168786398-168786568 | Rare:39 | ||||
| chr2:168890383-168890570 | Common:2; Rare:44 | ||||
| chr2:169362535-169362727 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 |