| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:160062474-160062722 | Common:5; Rare:64 | ||||
| chr2:160493432-160493595 | Common:1; Rare:56 | ||||
| chr2:161160235-161160485 | Common:2; Rare:73 | ||||
| chr2:164841199-164841550 | Rare:102 | ||||
| chr2:164841805-164841879 | Common:1; Rare:18 | ||||
| chr2:165794116-165794367 | Common:2; Rare:69; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794670-165794947 | Common:1; Rare:49 | ||||
| chr2:169362458-169362727 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169584715-169584811 | Rare:24 | ||||
| chr2:169694354-169694590 | Common:5; Rare:80 | ||||
| chr2:170928902-170929338 | Common:5; Rare:128 | ||||
| chr2:171160302-171160634 | Common:1; Rare:114 | ||||
| chr2:171433955-171434234 | Common:2; Rare:71 | ||||
| chr2:171434729-171434789 | Rare:15 | ||||
| chr2:171687118-171687537 | Common:3; Rare:74 |