| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128488484-128488640 | Common:1; Rare:34 | ||||
| chr3:128493193-128493442 | Rare:81 | ||||
| chr3:128879425-128879694 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129161013-129161228 | Common:1; Rare:72 | ||||
| chr3:129183784-129184075 | Common:2; Rare:99 | ||||
| chr3:129249554-129249683 | Common:1; Rare:39 | ||||
| chr3:129278777-129278882 | Common:3; Rare:30 | ||||
| chr3:129316251-129316315 | Rare:38 | ||||
| chr3:129439847-129440279 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893535-129893887 | Rare:136 | ||||
| chr3:130893905-130894257 | Common:3; Rare:103 | ||||
| chr3:131026723-131026909 | Common:2; Rare:46 | ||||
| chr3:131381529-131381811 | Common:2; Rare:67 | ||||
| chr3:131502809-131503006 | Common:1; Rare:92 | ||||
| chr3:132317221-132317583 | Rare:85 |