Variant report

Variant	rs12348134
Chromosome Location	chr9:110753105-110753106
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110749600-110757600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr9:110750800-110754800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr9:110751200-110755200	Enhancers	Primary B cells from cord blood	blood
4	chr9:110752000-110753200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:110752400-110753600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:110752400-110753800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:110752400-110754000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:110752400-110757600	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr9:110752600-110753800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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