Variant report

Variant	rs73026836
Chromosome Location	chr3:161849602-161849603
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12106720	1.00[EUR][1000 genomes]
rs55971156	1.00[EUR][1000 genomes]
rs56317862	1.00[EUR][1000 genomes]
rs56852494	1.00[EUR][1000 genomes]
rs57482426	1.00[EUR][1000 genomes]
rs59589204	1.00[EUR][1000 genomes]
rs73024767	1.00[EUR][1000 genomes]
rs73026863	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73875974	1.00[EUR][1000 genomes]
rs73875976	1.00[EUR][1000 genomes]
rs73875977	1.00[EUR][1000 genomes]
rs73875978	1.00[EUR][1000 genomes]
rs73875979	1.00[EUR][1000 genomes]
rs73875982	1.00[EUR][1000 genomes]
rs73875985	1.00[EUR][1000 genomes]
rs73875986	1.00[EUR][1000 genomes]
rs73875987	1.00[EUR][1000 genomes]
rs73875988	1.00[EUR][1000 genomes]
rs73875989	1.00[EUR][1000 genomes]
rs73875990	1.00[EUR][1000 genomes]
rs73875991	1.00[EUR][1000 genomes]
rs73875997	1.00[EUR][1000 genomes]
rs73878504	1.00[EUR][1000 genomes]
rs73878506	1.00[EUR][1000 genomes]
rs73878510	1.00[EUR][1000 genomes]
rs73878511	1.00[EUR][1000 genomes]
rs73878513	1.00[EUR][1000 genomes]
rs73878515	1.00[EUR][1000 genomes]
rs73878540	1.00[EUR][1000 genomes]
rs73878547	1.00[EUR][1000 genomes]
rs73878550	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460919	chr3:161799090-162094430	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv592144	chr3:161799090-162094430	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv877714	chr3:161807012-161854219	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
4	nsv877715	chr3:161807012-161862628	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv2753414	chr3:161826690-161935978	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv877717	chr3:161827760-161864213	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	n/a
7	nsv877718	chr3:161829492-161878713	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv877719	chr3:161847016-161903588	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 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	chr3:161848600-161853800	Weak transcription	Fetal Heart	heart

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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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