Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:23452688-23452824 | Rare:53; Clinvar (benign):1 | ||||
chr16:23557336-23557557 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641238-23641530 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24540392-24540494 | Rare:27 | ||||
chr16:24729620-24729758 | Common:7; Rare:73 | ||||
chr16:25015291-25015426 | Common:1; Rare:54 | ||||
chr16:25111520-25111845 | Common:2; Rare:101 | ||||
chr16:25258082-25258385 | Common:6; Rare:154 | ||||
chr16:27268719-27268875 | Common:1; Rare:54 | ||||
chr16:27549886-27550167 | Common:2; Rare:104 | ||||
chr16:28538639-28538754 | Rare:31 | ||||
chr16:28554188-28554275 | Common:1; Rare:28 | ||||
chr16:28822553-28822759 | Rare:76 | ||||
chr16:28823964-28824087 | Rare:30 | ||||
chr16:28846219-28846700 | Common:2; Rare:162; Clinvar:7; Clinvar (benign):6 |