| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:63912368-63912599 | Common:1; Rare:73 | ||||
| chr3:64023460-64023571 | Rare:41 | ||||
| chr3:64268039-64268439 | Rare:171 | ||||
| chr3:64687762-64687964 | Common:1; Rare:52 | ||||
| chr3:64687997-64688198 | Common:1; Rare:56 | ||||
| chr3:64688235-64688853 | Common:3; Rare:183 | ||||
| chr3:65597098-65597352 | Common:1; Rare:37 | ||||
| chr3:65597360-65597690 | Common:1; Rare:71 | ||||
| chr3:66038580-66039150 | Common:4; Rare:171 | ||||
| chr3:66220830-66221091 | Common:3; Rare:87 | ||||
| chr3:66501095-66501379 | Common:1; Rare:78 | ||||
| chr3:66998023-66998362 | Common:2; Rare:88 | ||||
| chr3:67654240-67654810 | Common:3; Rare:224 | ||||
| chr3:69009563-69009963 | Common:12; Rare:117; Clinvar (pathogenic):1 | ||||
| chr3:69013589-69013792 | Common:1; Rare:58 |