Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:167734819-167735071 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
chr3:167735617-167735731 | Rare:27 | ||||
chr3:168095888-168096090 | Rare:70 | ||||
chr3:169769549-169769645 | Rare:35 | ||||
chr3:169773343-169773425 | Rare:25 | ||||
chr3:170358143-170358467 | Common:3; Rare:113 | ||||
chr3:170421144-170421289 | Common:2; Rare:32 | ||||
chr3:170870163-170870207 | Rare:34 | ||||
chr3:170870209-170870280 | Rare:28 | ||||
chr3:170908584-170908841 | Common:1; Rare:72 | ||||
chr3:172039465-172039683 | Common:1; Rare:77 | ||||
chr3:172040260-172040616 | Common:3; Rare:89 | ||||
chr3:172711063-172711314 | Rare:68 | ||||
chr3:172750563-172750784 | Common:3; Rare:62 | ||||
chr3:174440811-174441010 | Common:2; Rare:53 |