Variant report

Variant	rs17444612
Chromosome Location	chr12:40788777-40788778
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10506153	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10878244	1.00[ASN][1000 genomes]
rs10878246	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11564128	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11564175	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11564177	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11564203	1.00[ASN][1000 genomes]
rs11564204	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11564205	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11564207	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11564267	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11829088	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11834950	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1491936	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17128385	1.00[ASN][1000 genomes]
rs17443552	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17444096	1.00[ASN][1000 genomes]
rs17444542	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17465912	1.00[CHB][hapmap]
rs17466037	1.00[CHB][hapmap]
rs17466339	1.00[CHB][hapmap]
rs17466430	1.00[ASN][1000 genomes]
rs17467095	1.00[CHB][hapmap]
rs17491061	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17492082	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17492138	1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17519573	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17520251	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17520278	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1907632	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1907633	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2114567	1.00[ASN][1000 genomes]
rs55775102	1.00[ASN][1000 genomes]
rs56322620	1.00[ASN][1000 genomes]
rs57997594	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60776971	1.00[ASN][1000 genomes]
rs61007767	1.00[ASN][1000 genomes]
rs73094605	1.00[ASN][1000 genomes]
rs73100409	1.00[ASN][1000 genomes]
rs73100414	1.00[ASN][1000 genomes]
rs73110067	1.00[ASN][1000 genomes]
rs73110075	1.00[ASN][1000 genomes]
rs73115378	1.00[ASN][1000 genomes]
rs73115394	1.00[ASN][1000 genomes]
rs73115401	1.00[ASN][1000 genomes]
rs73117512	1.00[ASN][1000 genomes]
rs73119913	1.00[ASN][1000 genomes]
rs73275761	1.00[ASN][1000 genomes]
rs73279554	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73279557	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9705735	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832377	chr12:40704881-40855223	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv899032	chr12:40735939-40827479	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv558598	chr12:40742363-40828264	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv1047639	chr12:40774370-40804386	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40787200-40799200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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