Variant report

Variant	rs1940639
Chromosome Location	chr11:94359567-94359568
allele	C/T
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	chr11:94347600-94359600	Weak transcription	Adipose Nuclei	Adipose
2	chr11:94354000-94359600	Weak transcription	Aorta	Aorta
3	chr11:94356000-94360200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr11:94357000-94363800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:94358400-94359600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:94358400-94360200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
7	chr11:94358600-94359800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:94359200-94361800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr11:94359400-94359600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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