| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001454-143001635 | Common:2; Rare:64 | ||||
| chr3:149129549-149129744 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:150408079-150408361 | Common:2; Rare:103 | ||||
| chr3:150603162-150603305 | Common:1; Rare:46 | ||||
| chr3:150703403-150703542 | Rare:39 | ||||
| chr3:151278304-151278497 | Common:2; Rare:40 | ||||
| chr3:152269636-152269654 | Rare:3 | ||||
| chr3:154324375-154324619 | Rare:90 | ||||
| chr3:155854361-155854748 | Rare:107 | ||||
| chr3:156674373-156674637 | Common:3; Rare:75 | ||||
| chr3:156826033-156826359 | Common:3; Rare:88 | ||||
| chr3:157149387-157149524 | Rare:30 | ||||
| chr3:157149619-157150159 | Common:1; Rare:131 | ||||
| chr3:157152554-157152626 | Rare:10 | ||||
| chr3:157153775-157153990 | Rare:32 |