| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159732242-159732392 | Common:1; Rare:26 | ||||
| chr3:165885565-165885829 | Common:5; Rare:58 | ||||
| chr3:169765051-169765215 | Rare:71; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr3:176321567-176321788 | Rare:48 | ||||
| chr3:176323129-176323220 | Common:1; Rare:17 | ||||
| chr3:176324547-176324860 | Common:6; Rare:56 | ||||
| chr3:176324968-176325002 | Common:1; Rare:7 | ||||
| chr3:176326483-176326486 | Rare:1 | ||||
| chr3:176326824-176327336 | Common:10; Rare:98 | ||||
| chr3:178860324-178860544 | Common:3; Rare:61 | ||||
| chr3:181712828-181713266 | Common:1; Rare:128; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr3:183447367-183447674 | Common:3; Rare:79 | ||||
| chr3:185786331-185786634 | Common:1; Rare:69 | ||||
| chr3:187175897-187175928 | Common:1; Rare:10 | ||||
| chr3:187466398-187466419 | Rare:5 |