| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123202238-123203194 | Common:11; Rare:196 | ||||
| chr3:123449087-123449391 | Rare:78 | ||||
| chr3:123449940-123450290 | Common:1; Rare:83 | ||||
| chr3:123584933-123585386 | Common:9; Rare:391 | ||||
| chr3:123585397-123585796 | Common:5; Rare:144 | ||||
| chr3:123884268-123884473 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:123961121-123961680 | Common:9; Rare:479 | ||||
| chr3:124504551-124504951 | Common:1; Rare:107 | ||||
| chr3:124584537-124584793 | Common:2; Rare:121 | ||||
| chr3:124584863-124585263 | Common:1; Rare:119 | ||||
| chr3:124730301-124730603 | Common:9; Rare:306; Clinvar:11; Clinvar (benign):9 | ||||
| chr3:124730660-124731114 | Common:4; Rare:147 | ||||
| chr3:124886781-124887000 | Common:4; Rare:80 | ||||
| chr3:124887172-124887691 | Common:5; Rare:342 | ||||
| chr3:125055979-125056255 | Rare:183 |