Variant report
Variant | rs6935642 |
---|---|
Chromosome Location | chr6:119435832-119435833 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:119431800-119438800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr6:119432400-119440800 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
3 | chr6:119434600-119438200 | Weak transcription | HepG2 | liver |
4 | chr6:119434600-119438200 | Weak transcription | K562 | blood |
5 | chr6:119434600-119440200 | Weak transcription | H9 Cell Line | embryonic stem cell |
6 | chr6:119434600-119443400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
7 | chr6:119434800-119439800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
8 | chr6:119435000-119440400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
9 | chr6:119435800-119436000 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |