| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141738024-141738422 | Common:2; Rare:165 | ||||
| chr3:141875989-141876246 | Rare:71 | ||||
| chr3:141876480-141876787 | Common:3; Rare:130 | ||||
| chr3:142225462-142225678 | Common:3; Rare:76 | ||||
| chr3:142578682-142578963 | Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596247-142596482 | Common:3; Rare:63 | ||||
| chr3:142888875-142889034 | Common:3; Rare:49 | ||||
| chr3:143001427-143001631 | Common:3; Rare:75 | ||||
| chr3:143119649-143119855 | Common:1; Rare:60 | ||||
| chr3:143971527-143971857 | Common:3; Rare:123 | ||||
| chr3:146160865-146161388 | Common:2; Rare:163; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250579-146251264 | Common:5; Rare:152 | ||||
| chr3:146469531-146469601 | Rare:14 | ||||
| chr3:146544465-146544797 | Common:5; Rare:80 | ||||
| chr3:146544814-146544896 | Rare:16 |