Variant report

Variant	rs6043271
Chromosome Location	chr20:15406913-15406914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16995985	1.00[EUR][1000 genomes]
rs16996043	1.00[EUR][1000 genomes]
rs16996120	1.00[EUR][1000 genomes]
rs6043262	1.00[GIH][hapmap];1.00[MEX][hapmap]
rs6043263	1.00[EUR][1000 genomes]
rs6043264	1.00[GIH][hapmap]
rs6043266	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6043274	1.00[GIH][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap]
rs6043280	1.00[EUR][1000 genomes]
rs6043281	1.00[EUR][1000 genomes]
rs6043382	1.00[EUR][1000 genomes]
rs6043383	1.00[EUR][1000 genomes]
rs741393	1.00[GIH][hapmap]
rs8123048	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062252	chr20:14964258-15547739	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv544206	chr20:14964258-15547739	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv833927	chr20:15362602-15520185	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	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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