Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:46762512-46762669 | Common:3; Rare:54 | ||||
chr22:50582806-50583142 | Common:6; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
chr22:50783611-50783859 | Common:2; Rare:74 | ||||
chr3:3126775-3127016 | Common:4; Rare:109; Clinvar (benign):4 | ||||
chr3:8501649-8501854 | Rare:71 | ||||
chr3:9362998-9363127 | Rare:45 | ||||
chr3:9397437-9397688 | Common:1; Rare:92 | ||||
chr3:9792398-9792570 | Rare:47 | ||||
chr3:9792740-9793112 | Common:3; Rare:128 | ||||
chr3:9843968-9844147 | Common:2; Rare:69 | ||||
chr3:9916963-9917154 | Common:2; Rare:42 | ||||
chr3:9933546-9933868 | Common:2; Rare:130; Clinvar:2 | ||||
chr3:10026329-10026484 | Rare:45 | ||||
chr3:10115524-10115712 | Common:3; Rare:69 | ||||
chr3:11643885-11643967 | Rare:29 |