| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27663507-27663926 | Rare:145 | ||||
| chr2:27890406-27890829 | Rare:109 | ||||
| chr2:28751701-28752175 | Common:2; Rare:195 | ||||
| chr2:28870262-28870437 | Rare:66 | ||||
| chr2:30146600-30147016 | Common:5; Rare:134 | ||||
| chr2:31234009-31234120 | Rare:30 | ||||
| chr2:32039743-32039851 | Rare:34 | ||||
| chr2:32165745-32165898 | Common:1; Rare:57 | ||||
| chr2:32627948-32628119 | Rare:54 | ||||
| chr2:33476547-33476682 | Common:2; Rare:23 | ||||
| chr2:33599204-33599442 | Common:1; Rare:90 | ||||
| chr2:37084269-37084561 | Common:4; Rare:110 | ||||
| chr2:37231535-37231703 | Common:4; Rare:94; Clinvar (benign):3 | ||||
| chr2:38076147-38076375 | Common:1; Rare:53 | ||||
| chr2:38377243-38377361 | Rare:51 |