Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:21952981-21953419 | Common:1; Rare:110; Clinvar (benign):3 | ||||
chr16:22008063-22008144 | Rare:27 | ||||
chr16:23452965-23453204 | Rare:68 | ||||
chr16:23557312-23557562 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
chr16:23641223-23641533 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24554612-24554758 | Common:2; Rare:29 | ||||
chr16:24729503-24729753 | Common:6; Rare:107 | ||||
chr16:25111453-25111789 | Common:2; Rare:86 | ||||
chr16:27268719-27268872 | Common:1; Rare:52 | ||||
chr16:27549891-27550167 | Common:2; Rare:101 | ||||
chr16:28538821-28538863 | Rare:11 | ||||
chr16:28824111-28824545 | Common:4; Rare:142 | ||||
chr16:28846271-28846643 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):5 | ||||
chr16:28863496-28863552 | Rare:12 | ||||
chr16:28925166-28925394 | Rare:74 |