| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70258019-70258174 | Common:1; Rare:53 | ||||
| chr2:70274876-70275015 | Common:1; Rare:36 | ||||
| chr2:70293621-70293861 | Common:3; Rare:80 | ||||
| chr2:70978579-70978657 | Rare:29 | ||||
| chr2:70978970-70979143 | Common:3; Rare:50 | ||||
| chr2:70994336-70994439 | Common:3; Rare:21 | ||||
| chr2:70994606-70994653 | Rare:13 | ||||
| chr2:70994806-70994951 | Common:3; Rare:52 | ||||
| chr2:71068516-71068686 | Rare:84 | ||||
| chr2:71130225-71130698 | Common:7; Rare:139; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130738-71130806 | Rare:29 | ||||
| chr2:71227047-71227422 | Common:2; Rare:91 | ||||
| chr2:71276434-71276698 | Rare:106 | ||||
| chr2:72147723-72147895 | Rare:53 | ||||
| chr2:72515721-72515860 | Common:1; Rare:19 |