Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:17742529-17742952 | Common:4; Rare:153 | ||||
chr3:19946974-19947457 | Common:7; Rare:179 | ||||
chr3:20186204-20186415 | Common:2; Rare:67 | ||||
chr3:23202930-23203207 | Common:1; Rare:97 | ||||
chr3:23916878-23917233 | Rare:134 | ||||
chr3:23917673-23918031 | Common:2; Rare:96; Clinvar (benign):1 | ||||
chr3:25428103-25428391 | Rare:65 | ||||
chr3:25783371-25783640 | Common:2; Rare:90; Clinvar (benign):3 | ||||
chr3:25790008-25790112 | Common:3; Rare:40 | ||||
chr3:27369319-27369606 | Rare:63 | ||||
chr3:28241433-28241674 | Common:1; Rare:83 | ||||
chr3:28348618-28348741 | Rare:27 | ||||
chr3:28348779-28349203 | Common:4; Rare:134 | ||||
chr3:29280829-29281102 | Common:3; Rare:56 | ||||
chr3:30606339-30606508 | Rare:39 |