Variant report

Variant	rs569655959
Chromosome Location	chr2:209451563-209451564
allele	A/G
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	esv2493689	chr2:209451033-209452683	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3327660	chr2:209451057-209453055	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2340327	chr2:209451536-209452239	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv6403	chr2:209451553-209452278	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209438800-209459400	Weak transcription	K562	blood
2	chr2:209449400-209458800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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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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