| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169362524-169362849 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169584303-169584630 | Common:1; Rare:124 | ||||
| chr2:169584723-169584825 | Rare:28 | ||||
| chr2:169694308-169694621 | Common:6; Rare:118 | ||||
| chr2:170928978-170929352 | Common:4; Rare:116 | ||||
| chr2:171160346-171160634 | Common:1; Rare:96 | ||||
| chr2:171433934-171434254 | Common:3; Rare:82 | ||||
| chr2:171434728-171434824 | Rare:24 | ||||
| chr2:171522262-171522554 | Common:3; Rare:71 | ||||
| chr2:171522689-171522737 | Rare:14 | ||||
| chr2:171687927-171688016 | Common:1; Rare:17 | ||||
| chr2:171894211-171894393 | Rare:78; Clinvar:1 | ||||
| chr2:171922308-171922499 | Rare:75 | ||||
| chr2:171999830-171999985 | Common:1; Rare:63 | ||||
| chr2:172735674-172735984 | Common:2; Rare:82 |