| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:174440904-174441006 | Common:1; Rare:27 | ||||
| chr3:177196387-177196782 | Common:2; Rare:128 | ||||
| chr3:179148017-179148196 | Common:3; Rare:60 | ||||
| chr3:179347573-179347774 | Common:1; Rare:44 | ||||
| chr3:179451391-179451605 | Common:1; Rare:74 | ||||
| chr3:179604616-179604848 | Common:2; Rare:85 | ||||
| chr3:180602050-180602235 | Common:1; Rare:62 | ||||
| chr3:180679467-180679568 | Rare:20; Clinvar:2 | ||||
| chr3:180989618-180989838 | Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711565-181712004 | Rare:118 | ||||
| chr3:182980488-182980809 | Common:3; Rare:109 | ||||
| chr3:183099443-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183635348-183635740 | Common:5; Rare:95 | ||||
| chr3:183697733-183697909 | Rare:87 | ||||
| chr3:183884821-183884961 | Rare:58 |