Variant report
Variant | rs73784336 |
---|---|
Chromosome Location | chr5:124139475-124139476 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:124129000-124141600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr5:124132000-124141800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
3 | chr5:124132600-124141800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
4 | chr5:124137600-124141000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr5:124137600-124141800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
6 | chr5:124137600-124142000 | Weak transcription | Fetal Kidney | kidney |
7 | chr5:124138000-124141800 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
8 | chr5:124138400-124141000 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
9 | chr5:124139000-124140000 | Enhancers | K562 | blood |
10 | chr5:124139400-124140000 | Enhancers | Fetal Intestine Small | intestine |
11 | chr5:124139400-124140400 | Enhancers | Fetal Intestine Large | intestine |