Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:20806419-20806659 | Rare:78 | ||||
chr16:20900062-20900873 | Common:6; Rare:188 | ||||
chr16:21953030-21953425 | Common:1; Rare:99; Clinvar (benign):3 | ||||
chr16:22206014-22206326 | Common:1; Rare:84 | ||||
chr16:22436952-22437071 | Rare:45 | ||||
chr16:23557336-23557686 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641257-23641525 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
chr16:24729551-24729739 | Common:6; Rare:93 | ||||
chr16:25015318-25015461 | Common:2; Rare:52 | ||||
chr16:25111468-25111762 | Common:2; Rare:68 | ||||
chr16:27268713-27268872 | Common:1; Rare:57 | ||||
chr16:27549877-27550177 | Common:2; Rare:118 | ||||
chr16:28491938-28492121 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
chr16:28538733-28539086 | Common:1; Rare:103 | ||||
chr16:28823923-28824129 | Common:1; Rare:59 |