| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71130201-71130758 | Common:7; Rare:169; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:72334706-72334955 | Rare:43 | ||||
| chr2:73070568-73070755 | Common:3; Rare:53 | ||||
| chr2:73112856-73113067 | Common:3; Rare:55 | ||||
| chr2:73214538-73214844 | Common:4; Rare:93 | ||||
| chr2:73234140-73234380 | Common:2; Rare:69 | ||||
| chr2:73829280-73829478 | Common:4; Rare:46 | ||||
| chr2:74147819-74148154 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74362651-74363059 | Common:4; Rare:112; Clinvar:6; Clinvar (benign):8 | ||||
| chr2:74369161-74369517 | Common:3; Rare:112; Clinvar:5; Clinvar (benign):4 | ||||
| chr2:74371674-74371967 | Common:2; Rare:70; Clinvar:1 | ||||
| chr2:74421595-74421768 | Rare:58 | ||||
| chr2:74425194-74425434 | Rare:69 | ||||
| chr2:74439961-74440254 | Rare:56 | ||||
| chr2:74458296-74458549 | Common:1; Rare:75 |