| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123585489-123585546 | Rare:10 | ||||
| chr3:124584582-124584714 | Rare:23 | ||||
| chr3:124730351-124730468 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375237-125375448 | Rare:63 | ||||
| chr3:127598269-127598467 | Common:2; Rare:58 | ||||
| chr3:127823165-127823378 | Common:3; Rare:46 | ||||
| chr3:128052194-128052500 | Common:2; Rare:99 | ||||
| chr3:128487907-128488078 | Common:1; Rare:44 | ||||
| chr3:128879385-128879669 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161027-129161152 | Common:1; Rare:47 | ||||
| chr3:129183808-129184078 | Common:2; Rare:90 | ||||
| chr3:129249545-129249664 | Common:1; Rare:35 | ||||
| chr3:129278761-129278882 | Common:4; Rare:40 | ||||
| chr3:129316279-129316315 | Rare:20 | ||||
| chr3:129439916-129440328 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):1 |