| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123102452-123102804 | Common:2; Rare:83 | ||||
| chr3:123413115-123413294 | Common:1; Rare:33 | ||||
| chr3:123618814-123619152 | Common:1; Rare:62 | ||||
| chr3:124819748-124819919 | Common:1; Rare:37 | ||||
| chr3:125819874-125819940 | Rare:12 | ||||
| chr3:125916334-125916618 | Common:4; Rare:86 | ||||
| chr3:126356195-126356238 | Rare:10 | ||||
| chr3:126989310-126989514 | Common:1; Rare:69 | ||||
| chr3:127456654-127456858 | Common:2; Rare:42 | ||||
| chr3:127536251-127536329 | Rare:17 | ||||
| chr3:128055507-128055749 | Rare:53; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:128061788-128061983 | Rare:35 | ||||
| chr3:128069335-128069556 | Rare:56; Clinvar (pathogenic):1 | ||||
| chr3:129004980-129005156 | Rare:27 | ||||
| chr3:129182922-129183224 | Common:1; Rare:81 |