| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134394465-134394769 | Common:3; Rare:57 | ||||
| chr3:138601738-138601912 | Rare:27 | ||||
| chr3:140708842-140709133 | Common:1; Rare:40 | ||||
| chr3:150408837-150409014 | Rare:53 | ||||
| chr3:151531357-151531704 | Common:3; Rare:52 | ||||
| chr3:152870307-152870472 | Rare:22 | ||||
| chr3:153762963-153763158 | Common:2; Rare:23 | ||||
| chr3:156816949-156817227 | Common:1; Rare:95 | ||||
| chr3:157174870-157174910 | Rare:16 | ||||
| chr3:169764840-169765139 | Common:1; Rare:101; Clinvar:18; Clinvar (pathogenic):5 | ||||
| chr3:185656322-185656710 | Rare:66 | ||||
| chr3:185658541-185658899 | Common:1; Rare:71 | ||||
| chr3:187740187-187740261 | Rare:15 | ||||
| chr3:187740837-187740934 | Rare:21 | ||||
| chr3:187741357-187741502 | Rare:25 |