Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:136862027-136862269 | Common:1; Rare:67 | ||||
chr3:138594202-138594468 | Rare:85 | ||||
chr3:138608649-138609127 | Common:1; Rare:112 | ||||
chr3:138834828-138834984 | Rare:50 | ||||
chr3:139389557-139389892 | Common:2; Rare:109 | ||||
chr3:139539425-139539788 | Common:4; Rare:124 | ||||
chr3:140941584-140941911 | Common:2; Rare:117 | ||||
chr3:141231652-141231907 | Common:2; Rare:89 | ||||
chr3:141368360-141368530 | Rare:35 | ||||
chr3:141402267-141402415 | Common:2; Rare:43 | ||||
chr3:141738060-141738353 | Common:2; Rare:130 | ||||
chr3:142447974-142448135 | Common:1; Rare:56 | ||||
chr3:142578708-142578987 | Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
chr3:142596282-142596482 | Common:2; Rare:52 | ||||
chr3:143001377-143001631 | Common:4; Rare:91 |