Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:15094247-15094450 | Rare:97 | ||||
chr16:19067445-19067696 | Common:5; Rare:103; Clinvar:1 | ||||
chr16:20806431-20806659 | Rare:72 | ||||
chr16:20899729-20899915 | Rare:37 | ||||
chr16:21233602-21233744 | Rare:34 | ||||
chr16:21952977-21953435 | Common:1; Rare:113; Clinvar (benign):3 | ||||
chr16:22436952-22437063 | Rare:41 | ||||
chr16:23641257-23641517 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
chr16:24729611-24729730 | Common:6; Rare:67 | ||||
chr16:25111544-25111805 | Common:2; Rare:73 | ||||
chr16:27268724-27268872 | Common:1; Rare:50 | ||||
chr16:27313627-27313954 | Common:7; Rare:84 | ||||
chr16:27549892-27550161 | Common:2; Rare:95 | ||||
chr16:28822529-28822749 | Common:1; Rare:77 | ||||
chr16:28846257-28846463 | Common:2; Rare:87; Clinvar:6; Clinvar (benign):6 |