| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:63864210-63864410 | Rare:91 | ||||
| chr3:63864410-63864780 | Common:4; Rare:119 | ||||
| chr3:63911996-63912146 | Rare:50 | ||||
| chr3:63912209-63912609 | Common:2; Rare:177 | ||||
| chr3:64023407-64023648 | Common:3; Rare:102 | ||||
| chr3:64267720-64268700 | Common:9; Rare:263 | ||||
| chr3:64445389-64445650 | Common:4; Rare:121 | ||||
| chr3:64687980-64688167 | Common:1; Rare:55 | ||||
| chr3:66038347-66038980 | Common:7; Rare:325 | ||||
| chr3:66039226-66039375 | Common:1; Rare:41 | ||||
| chr3:66220451-66221254 | Common:24; Rare:398; Clinvar (pathogenic):2 | ||||
| chr3:67654562-67654822 | Common:4; Rare:174 | ||||
| chr3:68932471-68932775 | Common:2; Rare:169 | ||||
| chr3:69013091-69013491 | Common:1; Rare:178 | ||||
| chr3:69013590-69013771 | Rare:50 |