| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169966647-169966842 | Common:1; Rare:77 | ||||
| chr3:170870163-170870252 | Rare:52 | ||||
| chr3:171460064-171460507 | Common:2; Rare:99 | ||||
| chr3:172750466-172750730 | Common:3; Rare:68 | ||||
| chr3:173397485-173397814 | Common:4; Rare:110 | ||||
| chr3:174440819-174441006 | Common:2; Rare:51 | ||||
| chr3:179347636-179347796 | Common:1; Rare:42 | ||||
| chr3:179451395-179451614 | Common:1; Rare:74 | ||||
| chr3:179604620-179604848 | Common:2; Rare:84 | ||||
| chr3:180036889-180037197 | Rare:78 | ||||
| chr3:180601960-180602302 | Common:1; Rare:106 | ||||
| chr3:180679467-180679563 | Rare:18; Clinvar:2 | ||||
| chr3:180989652-180989804 | Rare:64; Clinvar:1 | ||||
| chr3:181711749-181711996 | Rare:74 | ||||
| chr3:183099444-183099669 | Common:1; Rare:80; Clinvar:3; Clinvar (benign):5 |