Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:69762250-69762381 | Common:1; Rare:36 | ||||
chr16:70114133-70114393 | Common:3; Rare:93 | ||||
chr16:70251930-70252082 | Common:1; Rare:54 | ||||
chr16:70289434-70289772 | Common:3; Rare:136; Clinvar:1 | ||||
chr16:70299072-70299345 | Common:1; Rare:64 | ||||
chr16:70346759-70346982 | Common:2; Rare:110 | ||||
chr16:70523532-70523852 | Common:3; Rare:104; Clinvar (pathogenic):1 | ||||
chr16:71230664-71230759 | Rare:35 | ||||
chr16:71289313-71289468 | Common:1; Rare:48 | ||||
chr16:71564872-71565209 | Common:2; Rare:101 | ||||
chr16:71808109-71808418 | Common:1; Rare:85 | ||||
chr16:71808751-71809360 | Common:4; Rare:224 | ||||
chr16:71845920-71846023 | Common:1; Rare:33 | ||||
chr16:71883474-71883673 | Rare:62 | ||||
chr16:71883879-71884401 | Common:1; Rare:167 |