Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:14630188-14630367 | Rare:87 | ||||
chr16:14632695-14632995 | Common:1; Rare:106 | ||||
chr16:15047444-15047651 | Common:1; Rare:54 | ||||
chr16:15094237-15094409 | Common:1; Rare:84 | ||||
chr16:15395905-15396021 | Rare:41 | ||||
chr16:15639168-15639473 | Common:2; Rare:85 | ||||
chr16:15642471-15642708 | Common:1; Rare:57 | ||||
chr16:15643005-15643267 | Rare:77 | ||||
chr16:15721498-15721810 | Common:2; Rare:99; Clinvar:6; Clinvar (benign):3 | ||||
chr16:15741649-15741754 | Rare:38; Clinvar:1; Clinvar (benign):4 | ||||
chr16:15741776-15742007 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
chr16:15856939-15857091 | Common:2; Rare:29; Clinvar:1; Clinvar (benign):2 | ||||
chr16:17369708-17369819 | Rare:14 | ||||
chr16:18801456-18801830 | Common:4; Rare:132 | ||||
chr16:18925747-18925927 | Common:2; Rare:62 |