| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70086931-70087118 | Common:1; Rare:93 | ||||
| chr2:70087307-70087866 | Common:2; Rare:203 | ||||
| chr2:70087871-70088477 | Common:1; Rare:161 | ||||
| chr2:70190693-70190806 | Rare:30 | ||||
| chr2:70293650-70293848 | Common:2; Rare:68 | ||||
| chr2:70717687-70717898 | Common:2; Rare:36 | ||||
| chr2:71068537-71068686 | Rare:64 | ||||
| chr2:71129771-71129932 | Rare:32 | ||||
| chr2:71130220-71130698 | Common:7; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276457-71276636 | Rare:69 | ||||
| chr2:71453529-71453727 | Rare:40 | ||||
| chr2:73070512-73070599 | Common:1; Rare:15 | ||||
| chr2:73071685-73071848 | Common:2; Rare:67 | ||||
| chr2:73214191-73214279 | Common:1; Rare:34 | ||||
| chr2:73385689-73386079 | Common:4; Rare:187; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 |