| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170870170-170870290 | Rare:64 | ||||
| chr3:171771324-171771488 | Common:1; Rare:32 | ||||
| chr3:172750414-172750730 | Common:3; Rare:71 | ||||
| chr3:179147994-179148152 | Common:1; Rare:39 | ||||
| chr3:179347573-179347799 | Common:1; Rare:54 | ||||
| chr3:179604578-179604852 | Common:3; Rare:107 | ||||
| chr3:180602100-180602378 | Common:1; Rare:96 | ||||
| chr3:180989619-180989790 | Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793393-182793632 | Common:3; Rare:53 | ||||
| chr3:183099436-183099742 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183635514-183635708 | Common:2; Rare:61 | ||||
| chr3:184017864-184018103 | Common:1; Rare:75 | ||||
| chr3:184135221-184135403 | Common:2; Rare:56; Clinvar:5 | ||||
| chr3:184185923-184186208 | Common:4; Rare:108 | ||||
| chr3:184248877-184249021 | Rare:75; Clinvar:5; Clinvar (benign):2 |