Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:8797625-8797873 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr16:10944332-10944630 | Common:1; Rare:91 | ||||
chr16:11668195-11668517 | Common:3; Rare:137 | ||||
chr16:11851406-11851641 | Common:1; Rare:121 | ||||
chr16:11915370-11915726 | Common:5; Rare:135 | ||||
chr16:11915889-11916215 | Common:2; Rare:134 | ||||
chr16:11976629-11976794 | Rare:65 | ||||
chr16:14630200-14630413 | Rare:92 | ||||
chr16:14632735-14632995 | Common:1; Rare:87 | ||||
chr16:15395908-15396167 | Rare:98 | ||||
chr16:15643025-15643267 | Rare:74 | ||||
chr16:18801474-18801830 | Common:4; Rare:126 | ||||
chr16:18925732-18925927 | Common:2; Rare:65 | ||||
chr16:18926098-18926179 | Rare:29 | ||||
chr16:19067439-19067696 | Common:5; Rare:105; Clinvar:1 |