| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161160062-161160374 | Common:3; Rare:67 | ||||
| chr2:163735853-163736150 | Common:2; Rare:53 | ||||
| chr2:164840648-164840756 | Common:1; Rare:24 | ||||
| chr2:164841188-164841561 | Rare:108 | ||||
| chr2:164841789-164841951 | Common:1; Rare:46 | ||||
| chr2:166375889-166376331 | Common:5; Rare:114; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:169584303-169584630 | Common:1; Rare:124 | ||||
| chr2:169584744-169584816 | Rare:18 | ||||
| chr2:169694334-169694579 | Common:5; Rare:86 | ||||
| chr2:170928924-170929343 | Common:4; Rare:125 | ||||
| chr2:171160302-171160466 | Rare:64 | ||||
| chr2:171160495-171160560 | Rare:20 | ||||
| chr2:171433917-171434225 | Common:3; Rare:84 | ||||
| chr2:171999831-171999985 | Common:1; Rare:63 | ||||
| chr2:173075912-173075962 | Rare:12 |