Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:69339562-69339826 | Common:1; Rare:109; Clinvar (benign):1 | ||||
chr16:69424573-69424717 | Common:1; Rare:54 | ||||
chr16:69726437-69726806 | Common:3; Rare:97 | ||||
chr16:69762282-69762373 | Rare:20 | ||||
chr16:70114150-70114393 | Common:2; Rare:84 | ||||
chr16:70289419-70289773 | Common:3; Rare:143; Clinvar:1; Clinvar (benign):2 | ||||
chr16:70346761-70346971 | Common:2; Rare:103 | ||||
chr16:70523533-70523861 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
chr16:71808754-71809155 | Common:1; Rare:167 | ||||
chr16:71845886-71846029 | Common:2; Rare:47 | ||||
chr16:71895254-71895584 | Common:3; Rare:126 | ||||
chr16:72093597-72093957 | Rare:86 | ||||
chr16:74296661-74296938 | Rare:112 | ||||
chr16:74607070-74607192 | Rare:69 | ||||
chr16:74666809-74667116 | Common:5; Rare:112 |