Variant report

Variant	rs59877552
Chromosome Location	chr11:76119261-76119262
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76097200-76122000	Weak transcription	Fetal Stomach	stomach
2	chr11:76115600-76119600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:76118200-76120200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:76118800-76120400	Enhancers	Fetal Kidney	kidney
5	chr11:76119200-76119800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:76119200-76119800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:76119200-76119800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:76119200-76120000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr11:76119200-76120000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr11:76119200-76120200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:76119200-76120200	Enhancers	HUVEC	blood vessel
12	chr11:76119200-76120800	Enhancers	hESC Derived CD184+ Endoderm 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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