| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:72335378-72335580 | Rare:29 | ||||
| chr2:72825891-72826108 | Rare:69 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 | ||||
| chr2:73214209-73214279 | Common:1; Rare:31 | ||||
| chr2:73214512-73214554 | Rare:14 | ||||
| chr2:73233177-73233451 | Common:1; Rare:74 | ||||
| chr2:73234193-73234368 | Common:2; Rare:55 | ||||
| chr2:73385650-73386098 | Common:4; Rare:215; Clinvar:18; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73737276-73737589 | Common:3; Rare:103 | ||||
| chr2:73828804-73829037 | Common:1; Rare:54 | ||||
| chr2:73926718-73926936 | Common:2; Rare:113; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147836-74148115 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178817-74179026 | Common:2; Rare:60 | ||||
| chr2:74198434-74198629 | Rare:74 | ||||
| chr2:74374632-74374822 | Rare:41 |