Variant report

Variant	rs2796204
Chromosome Location	chr1:71669219-71669220
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1573060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs171403	1.00[AMR][1000 genomes]
rs189598	1.00[AMR][1000 genomes]
rs1935564	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2261391	1.00[AMR][1000 genomes]
rs2639327	1.00[AMR][1000 genomes]
rs2639341	1.00[AMR][1000 genomes]
rs2694947	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2694948	1.00[AMR][1000 genomes]
rs652791	1.00[AMR][1000 genomes]

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	nsv949599	chr1:71655652-72327802	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71665600-71672400	Weak transcription	Pancreas	Pancrea

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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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