| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158672566-158672852 | Common:4; Rare:70 | ||||
| chr3:158801767-158802155 | Common:4; Rare:127 | ||||
| chr3:159763922-159764201 | Common:2; Rare:82 | ||||
| chr3:160399195-160399307 | Rare:31; Clinvar:2 | ||||
| chr3:160565564-160565784 | Common:2; Rare:77 | ||||
| chr3:161105284-161105361 | Common:1; Rare:31 | ||||
| chr3:161221167-161221326 | Rare:49 | ||||
| chr3:167734835-167735187 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169773253-169773429 | Rare:62 | ||||
| chr3:172039435-172039662 | Common:1; Rare:69 | ||||
| chr3:172750414-172750735 | Common:3; Rare:72 | ||||
| chr3:174440819-174441006 | Common:2; Rare:51 | ||||
| chr3:179451367-179451625 | Common:1; Rare:89 | ||||
| chr3:179604628-179604891 | Common:2; Rare:105 | ||||
| chr3:180989671-180989815 | Rare:56; Clinvar:1 |