| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121285077-121285477 | Common:3; Rare:136 | ||||
| chr2:121530325-121530431 | Rare:34 | ||||
| chr2:121530383-121531390 | Common:78; Rare:2009; Clinvar (pathogenic):36 | ||||
| chr2:121648716-121649148 | Common:6; Rare:166 | ||||
| chr2:121649120-121649816 | Common:15; Rare:729 | ||||
| chr2:121649872-121650825 | Common:10; Rare:493 | ||||
| chr2:121736728-121737353 | Common:29; Rare:983 | ||||
| chr2:121755339-121755794 | Common:31; Rare:863 | ||||
| chr2:126655590-126655850 | Rare:97 | ||||
| chr2:126655820-126656290 | Common:5; Rare:463; Clinvar:2 | ||||
| chr2:126656332-126656624 | Rare:169 | ||||
| chr2:127064775-127065216 | Common:1; Rare:283 | ||||
| chr2:127106900-127107373 | Common:9; Rare:193; Clinvar:12; Clinvar (benign):4 | ||||
| chr2:127294050-127294340 | Common:14; Rare:491; Clinvar:6; Clinvar (benign):14 | ||||
| chr2:127387135-127387581 | Common:20; Rare:443 |