| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33476547-33476701 | Common:2; Rare:28 | ||||
| chr2:33599178-33599394 | Rare:85 | ||||
| chr2:36356445-36356623 | Rare:76 | ||||
| chr2:37084269-37084566 | Common:4; Rare:113 | ||||
| chr2:37212382-37212641 | Rare:55 | ||||
| chr2:37231529-37231732 | Common:4; Rare:118; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37324690-37324909 | Common:1; Rare:84 | ||||
| chr2:37671428-37671773 | Common:2; Rare:122 | ||||
| chr2:37672519-37672644 | Common:3; Rare:44 | ||||
| chr2:37925477-37925549 | Rare:29 | ||||
| chr2:38075952-38076301 | Common:1; Rare:86 | ||||
| chr2:38076370-38076385 | Rare:2 | ||||
| chr2:38602895-38603193 | Common:4; Rare:117 | ||||
| chr2:38875886-38876041 | Common:1; Rare:54 | ||||
| chr2:39120983-39121094 | Common:1; Rare:37 |