| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172711014-172711160 | Rare:71 | ||||
| chr3:172750488-172750794 | Common:3; Rare:83 | ||||
| chr3:177196453-177196547 | Rare:24 | ||||
| chr3:179147988-179148139 | Common:1; Rare:39 | ||||
| chr3:179347590-179347761 | Common:1; Rare:38 | ||||
| chr3:179562669-179562995 | Rare:106 | ||||
| chr3:179604630-179604873 | Common:2; Rare:91 | ||||
| chr3:180602032-180602242 | Common:1; Rare:71 | ||||
| chr3:180602408-180602584 | Rare:47 | ||||
| chr3:180912336-180912713 | Common:4; Rare:124 | ||||
| chr3:180989647-180989898 | Rare:88; Clinvar:1 | ||||
| chr3:181711735-181711986 | Rare:77 | ||||
| chr3:182793360-182793673 | Common:3; Rare:81 | ||||
| chr3:182980584-182980885 | Common:3; Rare:99 | ||||
| chr3:183099460-183099758 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):5 |