| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:177196387-177196772 | Common:2; Rare:124 | ||||
| chr3:177197129-177197408 | Rare:96 | ||||
| chr3:179147968-179148184 | Common:3; Rare:70 | ||||
| chr3:179347425-179347792 | Common:4; Rare:78 | ||||
| chr3:179451356-179451641 | Common:1; Rare:100 | ||||
| chr3:179604577-179604936 | Common:4; Rare:146 | ||||
| chr3:180036948-180037178 | Rare:60 | ||||
| chr3:180602100-180602301 | Common:1; Rare:67 | ||||
| chr3:180679426-180679552 | Rare:25; Clinvar:3 | ||||
| chr3:180989606-180989827 | Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711677-181712062 | Rare:100 | ||||
| chr3:182980967-182981202 | Rare:46 | ||||
| chr3:183099443-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183635497-183635743 | Common:4; Rare:66 | ||||
| chr3:183697671-183697947 | Common:2; Rare:115 |