| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348500-28348890 | Common:2; Rare:90 | ||||
| chr3:28348951-28349373 | Common:4; Rare:131 | ||||
| chr3:28349400-28349650 | Common:2; Rare:62 | ||||
| chr3:29280825-29281076 | Common:3; Rare:50 | ||||
| chr3:29281793-29282058 | Common:1; Rare:59 | ||||
| chr3:30606120-30606720 | Common:2; Rare:156; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:30894462-30894862 | Common:6; Rare:178 | ||||
| chr3:31532107-31532209 | Common:2; Rare:33 | ||||
| chr3:31532271-31532654 | Common:5; Rare:119 | ||||
| chr3:31532770-31533040 | Common:2; Rare:113 | ||||
| chr3:31533309-31534205 | Common:10; Rare:377 | ||||
| chr3:31981210-31981520 | Common:2; Rare:54 | ||||
| chr3:32106320-32106680 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32238557-32238740 | Common:2; Rare:54 | ||||
| chr3:32391662-32391915 | Common:4; Rare:76 |