| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160399169-160399316 | Rare:39; Clinvar:2 | ||||
| chr3:160399431-160399736 | Rare:88; Clinvar:3 | ||||
| chr3:160449516-160449871 | Common:1; Rare:105 | ||||
| chr3:160565275-160565868 | Common:3; Rare:196 | ||||
| chr3:167734816-167735243 | Common:4; Rare:141; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735611-167735819 | Rare:54; Clinvar:1 | ||||
| chr3:168095110-168095275 | Rare:56 | ||||
| chr3:168095560-168095644 | Rare:19 | ||||
| chr3:169769549-169769791 | Common:2; Rare:81 | ||||
| chr3:169769796-169769906 | Common:2; Rare:22 | ||||
| chr3:169772747-169772868 | Rare:26 | ||||
| chr3:169773297-169773438 | Rare:53 | ||||
| chr3:169966732-169967032 | Common:4; Rare:100 | ||||
| chr3:170358200-170358611 | Common:4; Rare:138 | ||||
| chr3:170359550-170359788 | Common:1; Rare:75 |