Variant report

Variant	rs6690591
Chromosome Location	chr1:86587793-86587794
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11161736	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs11161738	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11161741	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11161742	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11161743	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161744	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161746	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12023254	0.82[EUR][1000 genomes]
rs12024954	0.81[CEU][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12048065	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12048574	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12057841	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12057874	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12057993	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12075854	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12117437	0.92[CEU][hapmap]
rs12117849	0.82[EUR][1000 genomes]
rs12118936	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12120396	0.92[CEU][hapmap]
rs12567887	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1507266	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1507284	0.91[CEU][hapmap]
rs2039602	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2039603	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2039604	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2221587	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2390014	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs2892909	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4656122	0.92[CEU][hapmap]
rs55713534	0.82[EUR][1000 genomes]
rs55740735	0.89[EUR][1000 genomes]
rs55912038	0.82[EUR][1000 genomes]
rs57251624	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61802232	0.82[EUR][1000 genomes]
rs61802233	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61802236	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61802237	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61802242	0.83[ASN][1000 genomes]
rs61802243	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61802244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6576806	0.92[CEU][hapmap]
rs6663055	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6675364	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6675562	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6678131	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6686446	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6690902	0.82[EUR][1000 genomes]
rs67222626	0.82[EUR][1000 genomes]
rs72716178	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7550464	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7550559	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7550571	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1010312	chr1:86469730-86686426	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1012467	chr1:86494935-86686426	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1009092	chr1:86532988-86724805	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv535024	chr1:86532988-86724805	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv830481	chr1:86550274-86737290	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv2763578	chr1:86584695-86622285	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86585400-86590600	Weak transcription	Fetal Lung	lung
2	chr1:86585600-86588400	Weak transcription	Dnd41	blood

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