| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:236569557-236569828 | Common:8; Rare:49 | ||||
| chr2:237085748-237085955 | Common:2; Rare:77 | ||||
| chr2:238060741-238061069 | Common:4; Rare:101 | ||||
| chr2:238203591-238203805 | Common:3; Rare:92 | ||||
| chr2:238426662-238427067 | Common:6; Rare:118 | ||||
| chr2:239309210-239309293 | Rare:15 | ||||
| chr2:239401635-239401781 | Rare:77 | ||||
| chr2:240025225-240025429 | Common:2; Rare:73; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240136243-240136429 | Common:1; Rare:83 | ||||
| chr2:240560735-240560906 | Common:2; Rare:81 | ||||
| chr2:240561036-240561313 | Common:4; Rare:125 | ||||
| chr2:240998233-240998352 | Rare:20 | ||||
| chr2:240998505-240998618 | Rare:34 | ||||
| chr2:241102279-241102395 | Common:2; Rare:39 | ||||
| chr2:241149450-241149638 | Common:2; Rare:58 |