Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:200888568-200888629 | Rare:13 | ||||
chr2:200888970-200889471 | Common:3; Rare:158 | ||||
chr2:200963536-200963909 | Common:1; Rare:102 | ||||
chr2:201071454-201072078 | Rare:143 | ||||
chr2:201451375-201451914 | Common:3; Rare:133 | ||||
chr2:201642622-201642773 | Common:1; Rare:71; Clinvar (benign):1 | ||||
chr2:201643422-201643546 | Rare:43; Clinvar:4; Clinvar (benign):1 | ||||
chr2:201780783-201781256 | Common:4; Rare:141; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202238447-202238716 | Common:1; Rare:92; Clinvar:1 | ||||
chr2:202265620-202265819 | Rare:73 | ||||
chr2:202375973-202376585 | Common:4; Rare:210; Clinvar:2; Clinvar (benign):3 | ||||
chr2:202377401-202377507 | Rare:34; Clinvar:1 | ||||
chr2:202634658-202635066 | Common:6; Rare:132 | ||||
chr2:202870753-202871009 | Common:2; Rare:64 | ||||
chr2:202871412-202871599 | Common:3; Rare:61 |