Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:88691474-88691696 | Common:2; Rare:74 | ||||
chr2:95165645-95165828 | Rare:58 | ||||
chr2:95207456-95207558 | Rare:39 | ||||
chr2:95402433-95402757 | Rare:98 | ||||
chr2:96208195-96208418 | Rare:115 | ||||
chr2:96208767-96208954 | Common:4; Rare:78 | ||||
chr2:96265959-96266343 | Common:2; Rare:116; Clinvar:1 | ||||
chr2:96857915-96858265 | Common:2; Rare:126 | ||||
chr2:96870808-96870843 | Rare:7 | ||||
chr2:97663902-97664193 | Common:1; Rare:102 | ||||
chr2:98608409-98608636 | Common:1; Rare:99; Clinvar (benign):1 | ||||
chr2:99141141-99141345 | Common:1; Rare:78 | ||||
chr2:99141671-99141740 | Rare:17 | ||||
chr2:99154883-99155054 | Common:1; Rare:69; Clinvar (benign):2 | ||||
chr2:99180977-99181240 | Common:2; Rare:74 |