Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:18790234-18790457 | Common:4; Rare:83 | ||||
chr16:19067418-19067685 | Common:5; Rare:102; Clinvar:1 | ||||
chr16:20806437-20806542 | Rare:41 | ||||
chr16:21953003-21953429 | Common:1; Rare:106; Clinvar (benign):3 | ||||
chr16:23453163-23453214 | Rare:15 | ||||
chr16:23557291-23557529 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):3 | ||||
chr16:23641242-23641555 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):3 | ||||
chr16:25111474-25111762 | Common:2; Rare:67 | ||||
chr16:27268724-27268872 | Common:1; Rare:50 | ||||
chr16:27313846-27313985 | Common:2; Rare:42 | ||||
chr16:27549861-27550158 | Common:2; Rare:111 | ||||
chr16:28822594-28822729 | Rare:52 | ||||
chr16:28846271-28846746 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5 | ||||
chr16:28863484-28863573 | Rare:16 | ||||
chr16:28925162-28925412 | Rare:79 |