Variant report

Variant	rs6666452
Chromosome Location	chr1:76913462-76913463
allele	A/G
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:17)

rs_ID	r²[population]
rs10873887	0.93[CHB][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11586719	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12096789	0.84[CHB][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4414090	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4447031	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs4593881	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4949722	0.89[CHB][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6593541	0.93[CHB][hapmap];0.91[JPT][hapmap]
rs6657805	0.83[ASN][1000 genomes]
rs6671888	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6700771	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7413797	0.84[CHB][hapmap];0.83[EUR][1000 genomes]
rs7554005	0.85[CHB][hapmap];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9437151	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9437154	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9437445	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs9437448	0.80[CEU][hapmap];0.91[JPT][hapmap]

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	nsv870621	chr1:76620313-76997071	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv534168	chr1:76718950-77039352	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv462006	chr1:76826279-77042405	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv546585	chr1:76826279-77042405	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76913200-76914400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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