| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28751694-28752169 | Common:2; Rare:200 | ||||
| chr2:28870243-28870475 | Rare:100 | ||||
| chr2:30146595-30147030 | Common:5; Rare:138 | ||||
| chr2:30147823-30148008 | Common:3; Rare:73 | ||||
| chr2:31234004-31234158 | Rare:40 | ||||
| chr2:31414683-31414937 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr2:32010517-32010818 | Rare:74 | ||||
| chr2:32010999-32011112 | Rare:33 | ||||
| chr2:32039285-32039580 | Rare:88 | ||||
| chr2:32039737-32039866 | Rare:40 | ||||
| chr2:32165730-32166011 | Common:3; Rare:112 | ||||
| chr2:32356940-32357225 | Common:4; Rare:113 | ||||
| chr2:33476547-33476665 | Common:2; Rare:20 | ||||
| chr2:33599202-33599445 | Common:1; Rare:91 | ||||
| chr2:37084258-37084563 | Common:4; Rare:112 |