Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:152268548-152269212 | Common:2; Rare:234 | ||||
chr3:152269549-152269689 | Rare:36 | ||||
chr3:155079859-155079904 | Rare:15 | ||||
chr3:155854355-155854765 | Rare:111 | ||||
chr3:155870386-155870727 | Rare:102 | ||||
chr3:156674353-156674647 | Common:3; Rare:88 | ||||
chr3:157160090-157160295 | Rare:87 | ||||
chr3:157543228-157543417 | Rare:42 | ||||
chr3:158571020-158571229 | Common:1; Rare:68 | ||||
chr3:158644487-158644664 | Common:5; Rare:67; Clinvar (benign):6 | ||||
chr3:158732174-158732357 | Common:6; Rare:49 | ||||
chr3:158801802-158802178 | Common:3; Rare:131 | ||||
chr3:159763926-159764221 | Common:2; Rare:84 | ||||
chr3:159764328-159764562 | Common:1; Rare:63 | ||||
chr3:159852997-159853266 | Rare:48 |