Variant report

Variant	rs542062499
Chromosome Location	chr11:83287963-83287964
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3373640	chr11:83287329-83290177	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
2	esv3327721	chr11:83287679-83290202	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83279000-83289800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:83279200-83291200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:83283800-83291400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:83286400-83290000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:83286400-83294200	Weak transcription	NHEK	skin
6	chr11:83287600-83288000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr11:83287600-83288000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr11:83287800-83288000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:83287800-83288000	Enhancers	Brain Hippocampus Middle	brain

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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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