| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70293654-70293852 | Common:3; Rare:66 | ||||
| chr2:71068533-71068654 | Rare:57 | ||||
| chr2:71130223-71130698 | Common:7; Rare:139; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276469-71276613 | Rare:49 | ||||
| chr2:73214146-73214285 | Common:1; Rare:46 | ||||
| chr2:73385794-73386099 | Common:4; Rare:161; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:74147829-74148150 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178804-74179057 | Common:3; Rare:74 | ||||
| chr2:74198345-74198671 | Rare:122 | ||||
| chr2:74421582-74421767 | Rare:65 | ||||
| chr2:74454937-74455130 | Rare:54 | ||||
| chr2:74482990-74483119 | Rare:55 | ||||
| chr2:74507673-74507873 | Common:1; Rare:56 | ||||
| chr2:74529631-74529912 | Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74833859-74834161 | Rare:90 |