Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:169773328-169773437 | Rare:35 | ||||
chr3:169975366-169975675 | Common:2; Rare:49 | ||||
chr3:169982705-169983199 | Common:2; Rare:108 | ||||
chr3:174440767-174441006 | Common:2; Rare:58 | ||||
chr3:177196375-177196786 | Common:2; Rare:135 | ||||
chr3:177197445-177197690 | Common:1; Rare:61 | ||||
chr3:179347627-179347761 | Common:1; Rare:31 | ||||
chr3:179604622-179604816 | Common:1; Rare:62 | ||||
chr3:180989646-180989779 | Rare:58; Clinvar:1 | ||||
chr3:183884842-183885011 | Rare:62 | ||||
chr3:184017876-184018081 | Common:1; Rare:61 | ||||
chr3:184135223-184135395 | Common:2; Rare:53; Clinvar:5 | ||||
chr3:184155297-184155429 | Rare:45 | ||||
chr3:184176811-184177063 | Common:1; Rare:55 | ||||
chr3:184180648-184180917 | Rare:74 |