| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158801984-158802155 | Common:2; Rare:80 | ||||
| chr3:160399196-160399314 | Rare:33; Clinvar:1 | ||||
| chr3:160449743-160449993 | Common:2; Rare:77 | ||||
| chr3:160565342-160565784 | Common:2; Rare:155 | ||||
| chr3:160755408-160755608 | Common:1; Rare:68 | ||||
| chr3:161105046-161105344 | Common:3; Rare:88 | ||||
| chr3:161221196-161221326 | Rare:39 | ||||
| chr3:167734835-167735226 | Common:3; Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735593-167735741 | Rare:37 | ||||
| chr3:169773193-169773420 | Common:1; Rare:74 | ||||
| chr3:170870170-170870213 | Rare:32 | ||||
| chr3:179147937-179148196 | Common:4; Rare:82 | ||||
| chr3:179604622-179604903 | Common:2; Rare:115 | ||||
| chr3:180989620-180989796 | Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099397-183099717 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 |