| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:24495033-24495433 | Common:5; Rare:130 | ||||
| chr3:24495670-24495917 | Common:3; Rare:191 | ||||
| chr3:25427941-25428510 | Rare:680 | ||||
| chr3:25663680-25664092 | Common:5; Rare:132 | ||||
| chr3:25664042-25664664 | Common:7; Rare:293 | ||||
| chr3:25664600-25664800 | Common:2; Rare:34 | ||||
| chr3:25664795-25665220 | Common:17; Rare:574 | ||||
| chr3:25665240-25665650 | Common:6; Rare:117 | ||||
| chr3:25782720-25783151 | Common:2; Rare:187 | ||||
| chr3:25783317-25783747 | Common:14; Rare:704; Clinvar:1; Clinvar (benign):21 | ||||
| chr3:25783860-25784101 | Common:5; Rare:66 | ||||
| chr3:25784208-25784608 | Common:3; Rare:68 | ||||
| chr3:25789730-25790255 | Common:36; Rare:693 | ||||
| chr3:25790200-25790530 | Common:3; Rare:169 | ||||
| chr3:27484151-27484761 | Common:19; Rare:688 |