Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:69339568-69339821 | Common:1; Rare:99; Clinvar (benign):1 | ||||
chr16:69726437-69726724 | Common:3; Rare:77 | ||||
chr16:70114127-70114376 | Common:3; Rare:89 | ||||
chr16:70346783-70346957 | Common:1; Rare:88 | ||||
chr16:70523524-70523837 | Common:3; Rare:102; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:71808761-71809129 | Common:1; Rare:156 | ||||
chr16:71845895-71846014 | Common:2; Rare:38 | ||||
chr16:71895348-71895550 | Rare:61 | ||||
chr16:72093579-72093934 | Rare:89 | ||||
chr16:74296719-74296882 | Rare:63 | ||||
chr16:75433379-75433812 | Common:4; Rare:136 | ||||
chr16:75623228-75623410 | Common:3; Rare:61 | ||||
chr16:75647638-75647803 | Common:2; Rare:79; Clinvar:3 | ||||
chr16:77191143-77191213 | Common:1; Rare:32 | ||||
chr16:79600732-79600947 | Common:1; Rare:62 |