| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70087372-70087812 | Common:2; Rare:166 | ||||
| chr2:70257977-70258242 | Common:2; Rare:93 | ||||
| chr2:70293654-70293912 | Common:3; Rare:83 | ||||
| chr2:71068534-71068678 | Rare:66 | ||||
| chr2:71130216-71130667 | Common:6; Rare:126; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071707-73071848 | Common:2; Rare:52 | ||||
| chr2:73385609-73385860 | Common:2; Rare:97; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:73737300-73737609 | Common:3; Rare:102 | ||||
| chr2:73828896-73829029 | Rare:38 | ||||
| chr2:73926686-73926934 | Common:2; Rare:117; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147866-74148052 | Common:1; Rare:50; Clinvar:2 | ||||
| chr2:74178808-74179026 | Common:2; Rare:63 | ||||
| chr2:74421582-74421762 | Rare:63 | ||||
| chr2:74440419-74440669 | Rare:67 | ||||
| chr2:74458323-74458509 | Rare:57 |