Variant report

Variant	rs6954791
Chromosome Location	chr7:126653798-126653799
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs17864959	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17865063	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17865133	1.00[YRI][hapmap]
rs17865858	0.90[YRI][hapmap]
rs17866780	1.00[YRI][hapmap]
rs17866903	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17866956	1.00[YRI][hapmap]
rs17867020	0.90[YRI][hapmap]
rs17867256	1.00[YRI][hapmap]
rs17869343	1.00[AMR][1000 genomes]
rs17869416	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17875030	1.00[AMR][1000 genomes]
rs56742208	1.00[AMR][1000 genomes]
rs6959432	1.00[YRI][hapmap]
rs6964696	1.00[YRI][hapmap]
rs6976356	1.00[YRI][hapmap]
rs73723522	1.00[AMR][1000 genomes]
rs7786082	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758132	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2759562	chr7:126494789-126677843	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv427805	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv608379	chr7:126643692-126657545	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv971543	chr7:126653280-126657192	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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