Variant report

Variant	rs115107759
Chromosome Location	chr10:23434819-23434820
allele	C/T
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	esv3427167	chr10:23433696-23435794	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23433000-23437200	Weak transcription	Pancreas	Pancrea
2	chr10:23434800-23435000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:23434800-23435400	Bivalent/Poised TSS	HepG2	liver
4	chr10:23434800-23435400	Bivalent Enhancer	K562	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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