Variant report

Variant	rs1419482
Chromosome Location	chr7:126269978-126269979
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1008905	1.00[ASW][hapmap];0.82[CEU][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.91[GIH][hapmap];1.00[LWK][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs10279616	0.82[CEU][hapmap];0.85[CHB][hapmap];1.00[TSI][hapmap];0.82[EUR][1000 genomes]
rs11760596	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12538632	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12667118	0.84[EUR][1000 genomes]
rs12671690	0.97[ASN][1000 genomes]
rs12706737	0.97[ASN][1000 genomes]
rs12706739	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs13227344	0.95[ASN][1000 genomes]
rs13234319	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs13241597	0.97[ASN][1000 genomes]
rs13241983	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs13243112	0.82[CEU][hapmap];0.85[CHB][hapmap];0.80[JPT][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1419483	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1579214	1.00[ASW][hapmap];0.82[CEU][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.80[JPT][hapmap];1.00[LWK][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap]
rs17611244	0.82[CEU][hapmap]
rs1815973	0.82[CEU][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.84[GIH][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs1833071	0.97[ASN][1000 genomes]
rs2073863	0.92[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2237761	0.80[CHD][hapmap]
rs2237764	0.84[EUR][1000 genomes]
rs2237765	0.82[CEU][hapmap]
rs2283068	0.82[CEU][hapmap];0.92[CHB][hapmap];0.84[EUR][1000 genomes]
rs2283069	1.00[ASW][hapmap];0.82[CEU][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.91[GIH][hapmap];1.00[LWK][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs2299460	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2299492	1.00[ASW][hapmap];0.82[CEU][hapmap];0.85[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.80[JPT][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2299493	0.80[CHD][hapmap]
rs2402820	0.80[CHD][hapmap]
rs2896374	0.82[CEU][hapmap];0.85[CHB][hapmap];1.00[TSI][hapmap];0.82[EUR][1000 genomes]
rs34261190	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35009695	0.82[EUR][1000 genomes]
rs36198401	0.97[ASN][1000 genomes]
rs3808152	0.82[CEU][hapmap];0.83[CHB][hapmap];0.88[JPT][hapmap];0.82[EUR][1000 genomes]
rs3808153	0.82[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];0.84[EUR][1000 genomes]
rs4731317	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap]
rs4731321	0.82[CEU][hapmap];0.92[CHB][hapmap];0.80[JPT][hapmap];0.84[EUR][1000 genomes]
rs6467088	0.95[ASN][1000 genomes]
rs6467089	0.97[ASN][1000 genomes]
rs6960925	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][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	nsv529300	chr7:125669493-126587858	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1032938	chr7:126067684-126587859	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv539119	chr7:126067684-126587859	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv889187	chr7:126219766-126478190	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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