Variant report

Variant	rs73797048
Chromosome Location	chr5:151665497-151665498
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs55945305	1.00[AFR][1000 genomes]
rs56825916	0.83[AFR][1000 genomes]
rs56838880	0.83[AFR][1000 genomes]
rs57467196	1.00[AFR][1000 genomes]
rs58429100	1.00[AFR][1000 genomes]
rs58663632	0.83[AFR][1000 genomes]
rs59420569	1.00[AFR][1000 genomes]
rs6579931	0.83[AFR][1000 genomes]
rs73796838	0.95[AFR][1000 genomes]
rs73796851	0.93[AFR][1000 genomes]
rs73796852	0.93[AFR][1000 genomes]
rs73796868	0.83[AFR][1000 genomes]
rs73797041	1.00[AFR][1000 genomes]
rs73797043	1.00[AFR][1000 genomes]
rs73797047	1.00[AFR][1000 genomes]
rs73797050	0.95[AFR][1000 genomes]
rs73797051	1.00[AFR][1000 genomes]
rs73797052	1.00[AFR][1000 genomes]
rs73797053	1.00[AFR][1000 genomes]
rs73797054	1.00[AFR][1000 genomes]
rs73797055	1.00[AFR][1000 genomes]
rs73797056	1.00[AFR][1000 genomes]
rs73797057	1.00[AFR][1000 genomes]
rs73797058	1.00[AFR][1000 genomes]
rs73797060	1.00[AFR][1000 genomes]
rs73798513	0.83[AFR][1000 genomes]
rs73798515	0.83[AFR][1000 genomes]
rs73798928	1.00[AFR][1000 genomes]
rs73798929	1.00[AFR][1000 genomes]
rs73798930	1.00[AFR][1000 genomes]
rs7709660	0.95[AFR][1000 genomes]
rs7735575	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023828	chr5:151522149-151956217	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830519	chr5:151588627-151800192	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr5:151665400-151665600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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