| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68467255-68467688 | Common:2; Rare:120 | ||||
| chr2:69387088-69387419 | Common:1; Rare:97; Clinvar:3 | ||||
| chr2:69643609-69643852 | Rare:91 | ||||
| chr2:69829508-69829741 | Common:1; Rare:95 | ||||
| chr2:70086909-70087118 | Common:1; Rare:106 | ||||
| chr2:70087299-70087773 | Common:2; Rare:180 | ||||
| chr2:70257902-70258182 | Common:1; Rare:91 | ||||
| chr2:70293655-70293825 | Common:2; Rare:62 | ||||
| chr2:71068526-71068686 | Rare:75 | ||||
| chr2:71130188-71130677 | Common:6; Rare:142; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73070557-73070715 | Common:3; Rare:42 | ||||
| chr2:73385627-73385863 | Common:2; Rare:92; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:73828804-73829029 | Common:1; Rare:53 | ||||
| chr2:73926792-73927012 | Common:1; Rare:121; Clinvar:10; Clinvar (benign):3 | ||||
| chr2:74002573-74002732 | Common:2; Rare:64 |