Variant report
Variant | rs2407701 |
---|---|
Chromosome Location | chr13:50417382-50417383 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:50411400-50422000 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr13:50413000-50421600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
3 | chr13:50413400-50418600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
4 | chr13:50415000-50418200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
5 | chr13:50415000-50418400 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
6 | chr13:50415000-50420600 | Weak transcription | K562 | blood |
7 | chr13:50415400-50421600 | Weak transcription | HepG2 | liver |
8 | chr13:50415400-50421800 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
9 | chr13:50415600-50421800 | Weak transcription | H9 Cell Line | embryonic stem cell |
10 | chr13:50416600-50418200 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
11 | chr13:50417000-50417600 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |