| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73828769-73829065 | Common:5; Rare:189 | ||||
| chr2:73829090-73829690 | Common:9; Rare:239 | ||||
| chr2:73892835-73893044 | Common:1; Rare:39 | ||||
| chr2:73926668-73927029 | Common:6; Rare:430; Clinvar:30; Clinvar (benign):9 | ||||
| chr2:73927015-73927851 | Common:1; Rare:513; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):4 | ||||
| chr2:73985769-73986169 | Common:5; Rare:158 | ||||
| chr2:73986097-73986604 | Common:1; Rare:158 | ||||
| chr2:73986721-73987498 | Common:7; Rare:291 | ||||
| chr2:74002519-74002814 | Common:2; Rare:103 | ||||
| chr2:74003160-74003600 | Common:6; Rare:75 | ||||
| chr2:74147782-74148115 | Common:6; Rare:228; Clinvar:6; Clinvar (benign):5 | ||||
| chr2:74178140-74178456 | Rare:99 | ||||
| chr2:74178699-74179130 | Common:15; Rare:331 | ||||
| chr2:74198366-74199125 | Common:7; Rare:460 | ||||
| chr2:74199058-74199183 | Rare:27 |