| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218269615-218269679 | Rare:29 | ||||
| chr2:218270095-218270601 | Common:5; Rare:163; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:218287238-218287427 | Common:1; Rare:33 | ||||
| chr2:218568270-218568688 | Common:5; Rare:104 | ||||
| chr2:218568731-218568961 | Common:1; Rare:65 | ||||
| chr2:218659586-218659748 | Rare:36 | ||||
| chr2:218671974-218672348 | Common:2; Rare:93 | ||||
| chr2:219160545-219160580 | Rare:5 | ||||
| chr2:219176926-219177041 | Common:3; Rare:34 | ||||
| chr2:219229577-219229873 | Common:2; Rare:82 | ||||
| chr2:219245401-219245531 | Rare:36 | ||||
| chr2:219441905-219442064 | Rare:37 | ||||
| chr2:219498680-219498938 | Common:2; Rare:56 | ||||
| chr2:226835992-226836084 | Rare:33 | ||||
| chr2:227325203-227325361 | Common:4; Rare:50 |