Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:86563323-86563585 | Common:2; Rare:94 | ||||
chr2:88691441-88691844 | Common:2; Rare:156; Clinvar:1 | ||||
chr2:95165670-95165828 | Rare:47 | ||||
chr2:95402612-95402767 | Rare:50 | ||||
chr2:96208236-96208459 | Rare:114 | ||||
chr2:96208761-96208954 | Common:4; Rare:79 | ||||
chr2:96265964-96266328 | Common:2; Rare:107; Clinvar:1 | ||||
chr2:97663982-97664100 | Rare:38 | ||||
chr2:98608418-98608654 | Common:1; Rare:103; Clinvar (benign):1 | ||||
chr2:99154886-99155045 | Common:1; Rare:66; Clinvar (benign):2 | ||||
chr2:99180985-99181239 | Common:2; Rare:72 | ||||
chr2:99336092-99336118 | Rare:5 | ||||
chr2:101252643-101252974 | Common:5; Rare:114 | ||||
chr2:101474686-101474894 | Common:1; Rare:39 | ||||
chr2:102736671-102736935 | Common:1; Rare:121 |