| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156674444-156674618 | Common:1; Rare:45 | ||||
| chr3:157160092-157160328 | Rare:100 | ||||
| chr3:158801802-158802146 | Common:3; Rare:119 | ||||
| chr3:159763174-159763275 | Rare:18 | ||||
| chr3:160399204-160399307 | Rare:29; Clinvar:1 | ||||
| chr3:160399528-160399683 | Rare:33 | ||||
| chr3:160565564-160565784 | Common:2; Rare:77 | ||||
| chr3:169772722-169772797 | Rare:18 | ||||
| chr3:169773331-169773415 | Rare:25 | ||||
| chr3:172039461-172039656 | Common:1; Rare:64 | ||||
| chr3:179347595-179347788 | Common:1; Rare:49 | ||||
| chr3:179604594-179604864 | Common:3; Rare:110 | ||||
| chr3:180601994-180602240 | Common:1; Rare:81 | ||||
| chr3:180989618-180989782 | Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099444-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 |