Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:43089338-43089490 | Common:3; Rare:50 | ||||
chr22:43812230-43812432 | Common:2; Rare:66 | ||||
chr22:43955303-43955560 | Common:3; Rare:77 | ||||
chr22:45163682-45164008 | Common:4; Rare:117 | ||||
chr22:46053795-46053885 | Rare:32 | ||||
chr22:46250268-46250404 | Common:1; Rare:43 | ||||
chr22:46267861-46268037 | Common:1; Rare:56 | ||||
chr22:46296665-46296918 | Common:2; Rare:92 | ||||
chr22:46762503-46762669 | Common:3; Rare:60 | ||||
chr22:50582794-50583136 | Common:7; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
chr22:50783598-50783859 | Common:2; Rare:82 | ||||
chr3:3126775-3126979 | Common:4; Rare:87; Clinvar (benign):1 | ||||
chr3:8501666-8501935 | Common:2; Rare:98 | ||||
chr3:9362977-9363117 | Common:1; Rare:53 | ||||
chr3:9792414-9792570 | Rare:40 |