| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:64225310-64225690 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:64268100-64268380 | Rare:115 | ||||
| chr3:64445201-64446001 | Common:10; Rare:382 | ||||
| chr3:64685849-64686298 | Common:1; Rare:103 | ||||
| chr3:64686563-64687280 | Common:8; Rare:297 | ||||
| chr3:64687314-64687833 | Common:2; Rare:266 | ||||
| chr3:64687882-64688306 | Common:3; Rare:220 | ||||
| chr3:66038026-66039010 | Common:11; Rare:674 | ||||
| chr3:66039173-66039441 | Common:2; Rare:140 | ||||
| chr3:66220398-66221271 | Common:16; Rare:337; Clinvar (pathogenic):1 | ||||
| chr3:66500943-66501103 | Rare:69 | ||||
| chr3:66997986-66998393 | Common:2; Rare:182 | ||||
| chr3:67653840-67654252 | Common:5; Rare:144 | ||||
| chr3:67654416-67654811 | Common:7; Rare:370 | ||||
| chr3:68932520-68932782 | Common:1; Rare:76 |