Variant report

Variant	rs56336463
Chromosome Location	chr4:131017939-131017940
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10000116	0.96[ASN][1000 genomes]
rs10030169	0.95[ASN][1000 genomes]
rs10518563	0.88[AMR][1000 genomes]
rs11099035	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11099038	0.84[EUR][1000 genomes]
rs11940266	0.84[EUR][1000 genomes]
rs12186169	0.86[EUR][1000 genomes]
rs12498225	0.85[EUR][1000 genomes]
rs12500968	0.86[EUR][1000 genomes]
rs12505433	0.86[EUR][1000 genomes]
rs12505777	0.85[EUR][1000 genomes]
rs13105501	0.84[EUR][1000 genomes]
rs13108078	0.86[EUR][1000 genomes]
rs13115484	0.95[ASN][1000 genomes]
rs13116547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13116660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13134698	0.95[ASN][1000 genomes]
rs13147905	0.96[ASN][1000 genomes]
rs13151624	0.84[EUR][1000 genomes]
rs1389215	0.85[EUR][1000 genomes]
rs1472192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1472193	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1532248	0.95[ASN][1000 genomes]
rs1532249	0.95[ASN][1000 genomes]
rs1588147	0.95[ASN][1000 genomes]
rs1826506	0.84[EUR][1000 genomes]
rs1979691	0.85[EUR][1000 genomes]
rs2172477	0.85[EUR][1000 genomes]
rs2221618	0.93[ASN][1000 genomes]
rs2391598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2893313	0.85[EUR][1000 genomes]
rs34504424	0.86[EUR][1000 genomes]
rs34576180	0.84[EUR][1000 genomes]
rs35125754	0.85[EUR][1000 genomes]
rs35585617	0.84[EUR][1000 genomes]
rs4864337	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4864338	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4864362	0.85[EUR][1000 genomes]
rs55822013	0.84[EUR][1000 genomes]
rs61305695	0.84[EUR][1000 genomes]
rs62311018	0.86[EUR][1000 genomes]
rs6534767	0.87[EUR][1000 genomes]
rs6534768	0.85[EUR][1000 genomes]
rs6534769	0.84[EUR][1000 genomes]
rs6534770	0.84[EUR][1000 genomes]
rs6534771	0.85[EUR][1000 genomes]
rs67064782	0.83[EUR][1000 genomes]
rs6814064	0.84[EUR][1000 genomes]
rs6819814	0.84[EUR][1000 genomes]
rs6820157	0.84[EUR][1000 genomes]
rs6827267	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6835950	0.84[EUR][1000 genomes]
rs6836280	0.84[EUR][1000 genomes]
rs6837051	0.86[EUR][1000 genomes]
rs6853784	0.85[EUR][1000 genomes]
rs7660805	0.86[EUR][1000 genomes]
rs7662942	0.84[EUR][1000 genomes]
rs7668202	0.85[EUR][1000 genomes]
rs7668480	0.85[EUR][1000 genomes]
rs7672289	0.82[EUR][1000 genomes]
rs7691650	0.83[EUR][1000 genomes]
rs7694610	0.86[EUR][1000 genomes]
rs7699362	0.86[EUR][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	nsv595414	chr4:130983055-131024471	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv595415	chr4:130983605-131046911	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv595416	chr4:130998472-131834405	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2762461	chr4:131004382-131391658	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr4:131014600-131020000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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