| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218381897-218382241 | Common:3; Rare:68 | ||||
| chr2:218399531-218399779 | Common:1; Rare:112 | ||||
| chr2:218400339-218400607 | Common:10; Rare:87 | ||||
| chr2:218568209-218568694 | Common:6; Rare:122 | ||||
| chr2:218568731-218568955 | Common:1; Rare:63 | ||||
| chr2:218607579-218607927 | Common:3; Rare:57 | ||||
| chr2:218659339-218659750 | Common:4; Rare:97 | ||||
| chr2:218661274-218661420 | Rare:37; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr2:218671966-218672348 | Common:2; Rare:96 | ||||
| chr2:218984459-218984588 | Rare:24 | ||||
| chr2:219176854-219177119 | Common:4; Rare:82 | ||||
| chr2:219178136-219178517 | Common:7; Rare:144 | ||||
| chr2:219206704-219206936 | Rare:83 | ||||
| chr2:219217789-219218042 | Rare:55 | ||||
| chr2:219229549-219229905 | Common:2; Rare:115 |