Variant report

Variant	rs201304797
Chromosome Location	chr1:84310793-84310794
allele	-/TT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523508	chr1:84310193-84314754	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84281400-84316600	Weak transcription	Pancreas	Pancrea
2	chr1:84297600-84313000	Weak transcription	Aorta	Aorta
3	chr1:84306000-84310800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:84306000-84311200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:84308000-84310800	Weak transcription	Liver	Liver
6	chr1:84310200-84311200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:84310200-84311200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:84310400-84310800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr1:84310400-84311400	Strong transcription	Primary T cells from cord blood	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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