Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:68310922-68311084 | Common:1; Rare:80 | ||||
chr16:69132547-69132680 | Rare:57 | ||||
chr16:69339541-69339821 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
chr16:69726442-69726868 | Common:3; Rare:111 | ||||
chr16:69762251-69762360 | Common:1; Rare:30 | ||||
chr16:70114127-70114369 | Common:3; Rare:88 | ||||
chr16:70289440-70289634 | Rare:72; Clinvar:1 | ||||
chr16:70299071-70299242 | Common:1; Rare:35 | ||||
chr16:70346759-70346965 | Common:1; Rare:101 | ||||
chr16:70523532-70523879 | Common:3; Rare:112; Clinvar (pathogenic):1 | ||||
chr16:71845920-71846023 | Common:1; Rare:33 | ||||
chr16:71895475-71895584 | Common:1; Rare:39 | ||||
chr16:72093587-72093950 | Rare:91 | ||||
chr16:74296720-74296920 | Rare:85 | ||||
chr16:74607074-74607187 | Rare:62 |