Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67843943-67844032 | Rare:12 | ||||
chr16:68021433-68021592 | Common:1; Rare:37 | ||||
chr16:68104900-68105072 | Rare:27 | ||||
chr16:68738133-68738353 | Rare:64; Clinvar:7; Clinvar (benign):10 | ||||
chr16:69072371-69072663 | Common:3; Rare:45 | ||||
chr16:69566867-69566954 | Rare:19 | ||||
chr16:70616595-70616707 | Rare:31 | ||||
chr16:70620153-70620455 | Common:10; Rare:88 | ||||
chr16:70621084-70621203 | Common:1; Rare:34 | ||||
chr16:70621731-70621946 | Common:3; Rare:64 | ||||
chr16:70623589-70623825 | Common:8; Rare:73 | ||||
chr16:71626913-71627094 | Rare:42 | ||||
chr16:71745241-71745496 | Common:1; Rare:51 | ||||
chr16:71801636-71801916 | Common:3; Rare:65 | ||||
chr16:72664930-72665221 | Common:2; Rare:98 |