| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169764973-169765252 | Common:1; Rare:106; Clinvar:7; Clinvar (pathogenic):4 | ||||
| chr3:170062412-170062431 | Rare:1 | ||||
| chr3:170097348-170097433 | Rare:25 | ||||
| chr3:172135789-172136032 | Rare:43 | ||||
| chr3:172251065-172251295 | Common:1; Rare:48 | ||||
| chr3:177300260-177300659 | Common:1; Rare:76 | ||||
| chr3:180615263-180615317 | Rare:9 | ||||
| chr3:184015611-184015851 | Rare:30 | ||||
| chr3:184015915-184015974 | Rare:13 | ||||
| chr3:185418816-185419080 | Common:1; Rare:38 | ||||
| chr3:187065307-187065592 | Rare:48 | ||||
| chr3:187072680-187072863 | Rare:43 | ||||
| chr3:188190836-188190948 | Common:2; Rare:18 | ||||
| chr3:188199042-188199173 | Common:1; Rare:18 | ||||
| chr3:188266025-188266388 | Rare:72 |