Variant report

Variant	rs9487134
Chromosome Location	chr6:109842380-109842381
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109835400-109851400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:109835600-109844400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:109837400-109842600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:109837800-109842800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:109838600-109861400	Weak transcription	Thymus	Thymus
6	chr6:109839000-109844600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:109839000-109848200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr6:109842000-109843000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr6:109842000-109843400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:109842200-109842600	Enhancers	Primary neutrophils fromperipheralblood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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