| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134485386-134485766 | Rare:88 | ||||
| chr3:134485977-134486065 | Common:2; Rare:30 | ||||
| chr3:136862032-136862277 | Common:1; Rare:68 | ||||
| chr3:139389596-139389876 | Common:2; Rare:85 | ||||
| chr3:140942111-140942217 | Common:2; Rare:27 | ||||
| chr3:141231652-141231894 | Common:2; Rare:86 | ||||
| chr3:143001436-143001631 | Common:3; Rare:72 | ||||
| chr3:146251035-146251229 | Common:1; Rare:50 | ||||
| chr3:149129545-149129676 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377628-149377790 | Common:1; Rare:40 | ||||
| chr3:149377798-149377814 | Rare:3 | ||||
| chr3:150408828-150408998 | Rare:50 | ||||
| chr3:150603157-150603356 | Common:2; Rare:77 | ||||
| chr3:152268585-152269086 | Common:2; Rare:186 | ||||
| chr3:152269529-152269720 | Rare:56 |