| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161308370-161308519 | Common:2; Rare:38 | ||||
| chr2:164841185-164841529 | Rare:99 | ||||
| chr2:169510124-169510459 | Rare:93; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:169584303-169584624 | Common:1; Rare:122 | ||||
| chr2:169584751-169584816 | Rare:18 | ||||
| chr2:169694383-169694559 | Common:5; Rare:50 | ||||
| chr2:170928915-170929331 | Common:5; Rare:124 | ||||
| chr2:171433991-171434224 | Common:1; Rare:63 | ||||
| chr2:171522158-171522547 | Common:3; Rare:102 | ||||
| chr2:171999831-171999982 | Common:1; Rare:62 | ||||
| chr2:172427733-172427900 | Rare:58; Clinvar:2 | ||||
| chr2:173965281-173965518 | Common:1; Rare:86 | ||||
| chr2:174395599-174395797 | Common:2; Rare:66 | ||||
| chr2:174486987-174487394 | Common:2; Rare:99 | ||||
| chr2:175181509-175181754 | Common:5; Rare:89 |