| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129517264-129517608 | Common:7; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:130003068-130003226 | Common:1; Rare:35 | ||||
| chr3:130111422-130111561 | Rare:44 | ||||
| chr3:130119913-130119972 | Common:1; Rare:11 | ||||
| chr3:130276640-130276921 | Common:4; Rare:53 | ||||
| chr3:131361564-131361916 | Common:3; Rare:105 | ||||
| chr3:131394072-131394226 | Common:1; Rare:23 | ||||
| chr3:132396801-132397062 | Rare:59 | ||||
| chr3:133570281-133570472 | Common:3; Rare:29 | ||||
| chr3:133912369-133912514 | Rare:17 | ||||
| chr3:134037602-134037768 | Common:1; Rare:29 | ||||
| chr3:134069846-134069941 | Common:2; Rare:32 | ||||
| chr3:134850901-134851020 | Rare:32 | ||||
| chr3:134854495-134854544 | Rare:13 | ||||
| chr3:135038852-135039025 | Common:3; Rare:40 |