| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28895112-28895268 | Rare:47 | ||||
| chr2:29115170-29115640 | Common:4; Rare:174 | ||||
| chr2:29117851-29118230 | Rare:140 | ||||
| chr2:29130260-29130720 | Common:7; Rare:104 | ||||
| chr2:30146460-30147000 | Common:12; Rare:340 | ||||
| chr2:30447148-30447357 | Common:6; Rare:145 | ||||
| chr2:32010459-32010835 | Common:2; Rare:148 | ||||
| chr2:32039720-32039928 | Rare:115 | ||||
| chr2:32063320-32063740 | Common:3; Rare:266; Clinvar:2 | ||||
| chr2:32063760-32064029 | Common:2; Rare:216; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:32165665-32165926 | Common:2; Rare:184 | ||||
| chr2:32277750-32277991 | Common:2; Rare:111 | ||||
| chr2:32356903-32357252 | Common:8; Rare:287 | ||||
| chr2:32627983-32628125 | Rare:81 | ||||
| chr2:33599192-33599455 | Common:2; Rare:180 |