| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:64687980-64688350 | Common:1; Rare:99 | ||||
| chr3:65532328-65533526 | Common:23; Rare:461 | ||||
| chr3:65597042-65597442 | Common:2; Rare:105 | ||||
| chr3:65597424-65597624 | Rare:40 | ||||
| chr3:65597780-65598020 | Common:3; Rare:104 | ||||
| chr3:65598073-65598515 | Rare:251 | ||||
| chr3:66038539-66039160 | Common:9; Rare:357 | ||||
| chr3:66220541-66221095 | Common:12; Rare:286 | ||||
| chr3:66221122-66221522 | Common:7; Rare:128; Clinvar (pathogenic):1 | ||||
| chr3:66997497-66997897 | Common:2; Rare:60 | ||||
| chr3:66997946-66998370 | Common:6; Rare:473 | ||||
| chr3:66998541-66998941 | Common:2; Rare:166 | ||||
| chr3:66998871-66999271 | Rare:125 | ||||
| chr3:67654450-67654850 | Common:11; Rare:539 | ||||
| chr3:69012780-69013550 | Common:6; Rare:378 |