Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:23453159-23453215 | Rare:17 | ||||
chr16:23557336-23557475 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641229-23641530 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24256027-24256442 | Common:4; Rare:83 | ||||
chr16:24539285-24539590 | Common:1; Rare:95 | ||||
chr16:24729604-24729727 | Common:6; Rare:68 | ||||
chr16:25015329-25015372 | Rare:15 | ||||
chr16:25111521-25111812 | Common:2; Rare:85 | ||||
chr16:27268719-27268872 | Common:1; Rare:52 | ||||
chr16:27549886-27550167 | Common:2; Rare:104 | ||||
chr16:28553882-28553990 | Common:1; Rare:36 | ||||
chr16:28822606-28822749 | Rare:55 | ||||
chr16:28846271-28846623 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):5 | ||||
chr16:28925167-28925261 | Rare:23 | ||||
chr16:28974647-28974792 | Common:1; Rare:60 |