| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19933131-19933219 | Rare:13 | ||||
| chr2:19933419-19933729 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:20106822-20106960 | Common:2; Rare:39 | ||||
| chr2:20447687-20447816 | Rare:35 | ||||
| chr2:20447860-20448140 | Rare:103 | ||||
| chr2:20448348-20448878 | Common:3; Rare:138 | ||||
| chr2:20822201-20822226 | Rare:7 | ||||
| chr2:25997786-25998044 | Common:5; Rare:60 | ||||
| chr2:26000684-26000752 | Rare:16 | ||||
| chr2:26033515-26033580 | Rare:16 | ||||
| chr2:26355446-26355763 | Common:4; Rare:52 | ||||
| chr2:26412309-26412582 | Common:4; Rare:51 | ||||
| chr2:26724085-26724259 | Common:1; Rare:35 | ||||
| chr2:27207204-27207295 | Rare:27 | ||||
| chr2:27283014-27283157 | Rare:22 |