Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29995606-29995719 | Rare:51 | ||||
chr16:29996070-29996313 | Common:2; Rare:89 | ||||
chr16:30064345-30064502 | Common:1; Rare:28; Clinvar (benign):1 | ||||
chr16:30065566-30065944 | Rare:128 | ||||
chr16:30069495-30070022 | Common:1; Rare:197; Clinvar:6; Clinvar (benign):7 | ||||
chr16:30075875-30076080 | Common:1; Rare:69 | ||||
chr16:30183508-30183633 | Common:1; Rare:33 | ||||
chr16:30193662-30193913 | |||||
chr16:30355211-30355453 | Common:2; Rare:83 | ||||
chr16:30355849-30355936 | Rare:21 | ||||
chr16:30445871-30446153 | Common:1; Rare:53 | ||||
chr16:30534526-30534636 | Common:1; Rare:42 | ||||
chr16:30534834-30535089 | Common:3; Rare:83 | ||||
chr16:30610229-30610522 | Common:1; Rare:72 | ||||
chr16:30658624-30658719 | Rare:29 |