Variant report

Variant	rs61477638
Chromosome Location	chr12:40136830-40136831
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10047563	0.82[AFR][1000 genomes]
rs10219652	0.95[ASN][1000 genomes]
rs10783993	0.80[ASN][1000 genomes]
rs10783998	0.85[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs10784001	0.80[ASN][1000 genomes]
rs10784016	0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs10784034	0.95[ASN][1000 genomes]
rs10784051	0.81[ASN][1000 genomes]
rs10877335	0.87[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs10877369	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10877410	0.81[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs11173257	0.90[ASN][1000 genomes]
rs11173259	0.80[ASN][1000 genomes]
rs11173260	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs11173262	0.93[ASN][1000 genomes]
rs11173376	0.92[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11173394	0.82[ASN][1000 genomes]
rs11173401	0.80[ASN][1000 genomes]
rs11173423	0.82[ASN][1000 genomes]
rs11173424	0.80[ASN][1000 genomes]
rs11173428	0.82[ASN][1000 genomes]
rs11173433	0.81[ASN][1000 genomes]
rs11173434	0.82[ASN][1000 genomes]
rs11173440	0.82[ASN][1000 genomes]
rs11173446	0.82[ASN][1000 genomes]
rs11173459	0.82[ASN][1000 genomes]
rs11173494	0.80[ASN][1000 genomes]
rs11173546	0.80[AMR][1000 genomes]
rs12229418	0.80[ASN][1000 genomes]
rs12823801	0.92[ASN][1000 genomes]
rs12825223	0.93[ASN][1000 genomes]
rs4238072	0.81[ASN][1000 genomes]
rs4238073	0.81[ASN][1000 genomes]
rs4255599	0.80[ASN][1000 genomes]
rs4255600	0.81[ASN][1000 genomes]
rs4312128	0.81[ASN][1000 genomes]
rs4322461	0.81[ASN][1000 genomes]
rs4381428	0.80[ASN][1000 genomes]
rs4388963	0.95[ASN][1000 genomes]
rs4405390	0.82[ASN][1000 genomes]
rs4405391	0.80[ASN][1000 genomes]
rs4417382	0.80[ASN][1000 genomes]
rs4594067	0.80[ASN][1000 genomes]
rs4768168	0.80[ASN][1000 genomes]
rs4768169	0.82[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs4768170	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs57244766	0.92[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs58418587	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs58755301	0.90[ASN][1000 genomes]
rs61931185	0.80[ASN][1000 genomes]
rs61931208	0.81[ASN][1000 genomes]
rs61933102	0.83[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs61933154	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs61933157	0.83[ASN][1000 genomes]
rs6421195	0.84[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs6421196	0.89[AFR][1000 genomes]
rs6421197	0.85[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs6421198	0.80[ASN][1000 genomes]
rs6581263	0.84[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs6581265	0.80[ASN][1000 genomes]
rs6581266	0.85[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs6581270	0.87[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs6581271	0.87[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs6581272	0.80[ASN][1000 genomes]
rs6581294	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7136929	0.83[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs7296585	0.84[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs7301886	0.82[ASN][1000 genomes]
rs7308955	0.95[ASN][1000 genomes]
rs7485345	0.84[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs7486196	0.80[ASN][1000 genomes]
rs7486621	0.84[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs7956577	0.84[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs7959905	0.87[AFR][1000 genomes]
rs7961070	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531527	chr12:39680812-40182822	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1037457	chr12:39898349-40245401	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv541480	chr12:39898349-40245401	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv899024	chr12:40046408-40188870	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1053603	chr12:40082673-40197609	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv427907	chr12:40122713-40199621	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv428280	chr12:40122713-40199621	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40130800-40137000	Weak transcription	Liver	Liver
2	chr12:40130800-40156400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr12:40136800-40137200	ZNF genes & repeats	Aorta	Aorta

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