| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:181550682-181550798 | Rare:13 | ||||
| chr3:181699755-181699778 | Rare:3 | ||||
| chr3:181712817-181712882 | Rare:14; Clinvar (pathogenic):1 | ||||
| chr3:181952296-181952471 | Common:1; Rare:27 | ||||
| chr3:182182755-182182892 | Rare:24 | ||||
| chr3:182364977-182365071 | Common:1; Rare:24 | ||||
| chr3:183101532-183101691 | Rare:34 | ||||
| chr3:183447469-183447729 | Common:1; Rare:64 | ||||
| chr3:183464666-183464787 | Common:2; Rare:23 | ||||
| chr3:183810318-183810572 | Common:1; Rare:74 | ||||
| chr3:184229410-184229606 | Common:1; Rare:48 | ||||
| chr3:184259018-184259136 | Common:1; Rare:15 | ||||
| chr3:184359882-184360036 | Rare:40 | ||||
| chr3:184401497-184401589 | Rare:20 | ||||
| chr3:185418822-185418917 | Rare:7 |