| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44090648-44090864 | Common:3; Rare:43 | ||||
| chr2:44169638-44169802 | Common:1; Rare:45 | ||||
| chr2:44362698-44362708 | Rare:1 | ||||
| chr2:44778482-44778582 | Rare:19 | ||||
| chr2:44778728-44779090 | Rare:86 | ||||
| chr2:44779885-44779991 | Rare:17 | ||||
| chr2:44805493-44805587 | Common:5; Rare:41 | ||||
| chr2:44825811-44825969 | Common:1; Rare:27 | ||||
| chr2:44937879-44938062 | Common:1; Rare:46 | ||||
| chr2:44942435-44942656 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr2:44943453-44943481 | Rare:3 | ||||
| chr2:45290134-45290247 | Common:3; Rare:22 | ||||
| chr2:45610528-45610723 | Rare:47 | ||||
| chr2:45650004-45650166 | Common:1; Rare:54 | ||||
| chr2:45650532-45650689 | Common:1; Rare:33 |