Variant report

Variant	rs57488737
Chromosome Location	chr13:88786695-88786696
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs58920470	1.00[EUR][1000 genomes]
rs59535491	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7321533	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73571617	1.00[EUR][1000 genomes]
rs73571625	1.00[EUR][1000 genomes]
rs73578158	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73578163	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73578171	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73578179	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73579203	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73579212	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73579216	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73580123	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74104233	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900790	chr13:88585928-88891870	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv900792	chr13:88623302-88871759	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv900793	chr13:88711960-88871759	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1037729	chr13:88728499-89127873	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv541864	chr13:88728499-89127873	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv1806101	chr13:88771495-88910106	Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv1812668	chr13:88771495-88910106	Enhancers Weak transcription Active TSS	TF binding region CpG island lncRNA	3 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	chr13:88784400-88787000	Weak transcription	Primary T killer memory cells from peripheral blood	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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