Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:21599364-21599611 | Common:3; Rare:90 | ||||
chr16:21953028-21953440 | Common:1; Rare:103; Clinvar (benign):3 | ||||
chr16:23641247-23641526 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24540380-24540486 | Rare:29 | ||||
chr16:24729607-24729753 | Common:6; Rare:74 | ||||
chr16:24954604-24954836 | Common:1; Rare:55 | ||||
chr16:25015320-25015679 | Common:2; Rare:94 | ||||
chr16:25111474-25111760 | Common:2; Rare:67 | ||||
chr16:27268719-27268872 | Common:1; Rare:52 | ||||
chr16:27313804-27314023 | Common:2; Rare:59 | ||||
chr16:27340590-27340798 | Common:1; Rare:44 | ||||
chr16:27402375-27402541 | Common:1; Rare:30 | ||||
chr16:27549892-27550188 | Common:2; Rare:112 | ||||
chr16:28553823-28553990 | Common:1; Rare:55 | ||||
chr16:28824271-28824501 | Common:2; Rare:78 |