| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179604571-179604855 | Common:3; Rare:114 | ||||
| chr3:179652490-179652790 | Common:3; Rare:54 | ||||
| chr3:179653042-179653265 | Common:2; Rare:78 | ||||
| chr3:179653339-179653710 | Common:6; Rare:113 | ||||
| chr3:180601953-180602232 | Common:1; Rare:81 | ||||
| chr3:180679251-180680224 | Common:8; Rare:420; Clinvar:9 | ||||
| chr3:180912130-180912460 | Common:3; Rare:76 | ||||
| chr3:180912514-180912759 | Common:1; Rare:91 | ||||
| chr3:180913050-180913290 | Rare:72 | ||||
| chr3:180989637-180989945 | Rare:105; Clinvar:1 | ||||
| chr3:181711695-181712052 | Rare:95 | ||||
| chr3:182793315-182793602 | Common:3; Rare:82 | ||||
| chr3:182980476-182980657 | Rare:63 | ||||
| chr3:183099436-183099784 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183116007-183116280 | Common:3; Rare:72 |