| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164620980-164621275 | Rare:70 | ||||
| chr2:164840353-164840815 | Common:1; Rare:75 | ||||
| chr2:164841798-164842139 | Common:2; Rare:104 | ||||
| chr2:164955343-164955596 | Rare:54 | ||||
| chr2:165469540-165469717 | Rare:34 | ||||
| chr2:169362427-169362727 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169479393-169479558 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr2:169584290-169584630 | Common:1; Rare:129 | ||||
| chr2:169584734-169584816 | Rare:20 | ||||
| chr2:169694334-169694590 | Common:5; Rare:90 | ||||
| chr2:170928979-170929330 | Common:4; Rare:113 | ||||
| chr2:171160302-171160487 | Rare:72 | ||||
| chr2:171160491-171160665 | Common:1; Rare:49 | ||||
| chr2:171433922-171434248 | Common:3; Rare:85 | ||||
| chr2:171434714-171434740 | Rare:10 |