| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162838525-162838668 | Rare:39 | ||||
| chr2:162838672-162839128 | Common:1; Rare:97 | ||||
| chr2:163735987-163736069 | Rare:16 | ||||
| chr2:164840691-164840756 | Common:1; Rare:11 | ||||
| chr2:164955484-164955596 | Rare:24 | ||||
| chr2:165469539-165469722 | Rare:35 | ||||
| chr2:165572246-165572431 | Rare:31 | ||||
| chr2:165574125-165574320 | Rare:39 | ||||
| chr2:166375777-166376087 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:168456125-168456358 | Rare:78 | ||||
| chr2:169584303-169584624 | Common:1; Rare:122 | ||||
| chr2:169584744-169584809 | Rare:15 | ||||
| chr2:169694323-169694573 | Common:6; Rare:90 | ||||
| chr2:169798767-169798960 | Rare:51 | ||||
| chr2:170928915-170929313 | Common:5; Rare:115 |