| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:229921899-229922511 | Common:4; Rare:213 | ||||
| chr2:230225604-230225774 | Rare:37 | ||||
| chr2:230416077-230416231 | Rare:43 | ||||
| chr2:231707029-231707189 | Rare:37 | ||||
| chr2:231710278-231710519 | Common:2; Rare:120 | ||||
| chr2:231781247-231781476 | Rare:67 | ||||
| chr2:231961632-231961742 | Rare:30; Clinvar:1 | ||||
| chr2:232550550-232550723 | Rare:66 | ||||
| chr2:233854523-233854720 | Common:4; Rare:45 | ||||
| chr2:237085829-237085955 | Common:1; Rare:56 | ||||
| chr2:237487179-237487277 | Common:1; Rare:27 | ||||
| chr2:238060712-238061029 | Common:4; Rare:99 | ||||
| chr2:238203616-238203810 | Common:3; Rare:82 | ||||
| chr2:240025282-240025407 | Common:1; Rare:51; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:241102270-241102357 | Common:2; Rare:35 |