| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27890400-27890812 | Rare:105 | ||||
| chr2:28751728-28752134 | Common:1; Rare:166 | ||||
| chr2:28870268-28870425 | Rare:59 | ||||
| chr2:30147876-30147988 | Common:1; Rare:37 | ||||
| chr2:32039743-32039851 | Rare:34 | ||||
| chr2:32165711-32165920 | Common:1; Rare:85 | ||||
| chr2:36561441-36561849 | Common:3; Rare:85 | ||||
| chr2:37084319-37084566 | Common:3; Rare:96 | ||||
| chr2:37231559-37231722 | Common:4; Rare:93; Clinvar (benign):3 | ||||
| chr2:37324735-37324948 | Common:1; Rare:89 | ||||
| chr2:37344604-37344741 | Common:1; Rare:57 | ||||
| chr2:38875886-38876059 | Common:1; Rare:63 | ||||
| chr2:39437079-39437453 | Common:4; Rare:133 | ||||
| chr2:43595972-43596169 | Common:1; Rare:60 | ||||
| chr2:44361479-44361902 | Common:3; Rare:131 |