| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218270091-218270587 | Common:5; Rare:158; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218292482-218292644 | Common:1; Rare:49 | ||||
| chr2:218568227-218568640 | Common:5; Rare:109 | ||||
| chr2:218568668-218568957 | Common:1; Rare:77 | ||||
| chr2:218659474-218659755 | Common:2; Rare:70 | ||||
| chr2:218671977-218672305 | Common:2; Rare:81 | ||||
| chr2:218745914-218746104 | Common:1; Rare:27 | ||||
| chr2:219176907-219177114 | Common:4; Rare:63 | ||||
| chr2:219206681-219206916 | Rare:86 | ||||
| chr2:219229336-219229419 | Rare:28 | ||||
| chr2:219229544-219229893 | Common:2; Rare:110 | ||||
| chr2:219245416-219245531 | Rare:33 | ||||
| chr2:219253859-219254055 | Common:1; Rare:62 | ||||
| chr2:219279171-219279608 | Common:3; Rare:133; Clinvar (benign):1 | ||||
| chr2:219498670-219498917 | Common:2; Rare:49 |