Variant report

Variant	rs34720319
Chromosome Location	chr5:124627209-124627210
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882823	chr5:124569471-124639468	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1034696	chr5:124616571-124654771	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3361600	chr5:124626989-124628140	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
4	nsv823206	chr5:124627008-124628142	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124614400-124631400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:124622400-124628600	Weak transcription	Fetal Brain Male	brain
3	chr5:124624600-124628000	Enhancers	Liver	Liver
4	chr5:124627200-124627400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:124627200-124627600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:124627200-124627600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr5:124627200-124627800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:124627200-124627800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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