| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:30147629-30147999 | Common:4; Rare:143 | ||||
| chr2:30231286-30231574 | Common:1; Rare:93 | ||||
| chr2:30447049-30447359 | Common:5; Rare:108 | ||||
| chr2:32010204-32010443 | Rare:69 | ||||
| chr2:32010445-32010517 | Rare:17 | ||||
| chr2:32010706-32011250 | Common:1; Rare:160 | ||||
| chr2:32011255-32011417 | Common:1; Rare:34 | ||||
| chr2:32039500-32039578 | Rare:17 | ||||
| chr2:32039669-32040093 | Common:3; Rare:108 | ||||
| chr2:32063318-32063753 | Common:2; Rare:152; Clinvar:1 | ||||
| chr2:32063826-32064070 | Common:1; Rare:117; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:32165580-32166032 | Common:3; Rare:169 | ||||
| chr2:32264765-32264964 | Common:1; Rare:40 | ||||
| chr2:32265005-32265037 | Rare:6 | ||||
| chr2:32277725-32277990 | Common:1; Rare:62 |