| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128052161-128052520 | Common:2; Rare:121 | ||||
| chr3:128123702-128124051 | Rare:102 | ||||
| chr3:128487914-128488064 | Common:1; Rare:37 | ||||
| chr3:128488508-128488660 | Common:1; Rare:33 | ||||
| chr3:128493195-128493358 | Rare:51 | ||||
| chr3:128650763-128650924 | Common:1; Rare:71 | ||||
| chr3:128680633-128680862 | Common:2; Rare:69 | ||||
| chr3:128681127-128681302 | Common:1; Rare:53 | ||||
| chr3:128726037-128726219 | Common:1; Rare:50; Clinvar:3 | ||||
| chr3:128879346-128879675 | Common:5; Rare:153; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160979-129161488 | Common:3; Rare:161 | ||||
| chr3:129183758-129184135 | Common:2; Rare:143 | ||||
| chr3:129249524-129249682 | Common:2; Rare:49 | ||||
| chr3:129278743-129278898 | Common:4; Rare:45 | ||||
| chr3:129316268-129316360 | Common:1; Rare:34 |