| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70293645-70293835 | Common:2; Rare:67 | ||||
| chr2:70553801-70553852 | Common:1; Rare:16 | ||||
| chr2:70935754-70935943 | Common:3; Rare:41; Clinvar (benign):3 | ||||
| chr2:70994812-70994967 | Common:3; Rare:54 | ||||
| chr2:71068095-71068329 | Rare:64 | ||||
| chr2:71068523-71068710 | Rare:86 | ||||
| chr2:71129756-71129932 | Rare:36 | ||||
| chr2:71130220-71130682 | Common:6; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:72147702-72148004 | Rare:83 | ||||
| chr2:72148244-72148318 | Rare:11 | ||||
| chr2:72825798-72826081 | Rare:89 | ||||
| chr2:73070580-73070729 | Common:3; Rare:39 | ||||
| chr2:73234154-73234381 | Common:2; Rare:67 | ||||
| chr2:73828796-73829029 | Common:1; Rare:54 | ||||
| chr2:73926701-73926964 | Common:2; Rare:131; Clinvar:7; Clinvar (benign):3 |