Variant report

Variant	rs9329034
Chromosome Location	chr4:69642621-69642622
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10000284	0.82[EUR][1000 genomes]
rs10010381	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10010497	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10028938	0.86[EUR][1000 genomes]
rs11249508	0.84[AFR][1000 genomes]
rs11722451	0.88[EUR][1000 genomes]
rs11725000	0.99[EUR][1000 genomes]
rs11725119	0.82[EUR][1000 genomes]
rs11725502	0.83[EUR][1000 genomes]
rs11726045	0.97[EUR][1000 genomes]
rs11731269	0.90[EUR][1000 genomes]
rs11734565	0.91[EUR][1000 genomes]
rs11736654	0.99[EUR][1000 genomes]
rs11737527	0.88[EUR][1000 genomes]
rs11737644	0.84[EUR][1000 genomes]
rs11737672	0.88[EUR][1000 genomes]
rs11930531	0.82[AFR][1000 genomes]
rs1849536	0.84[AFR][1000 genomes]
rs1902932	0.84[EUR][1000 genomes]
rs2175776	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2331437	0.99[EUR][1000 genomes]
rs2331438	0.99[EUR][1000 genomes]
rs2331439	0.99[EUR][1000 genomes]
rs2331559	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2926036	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2926038	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2942856	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294759	0.93[EUR][1000 genomes]
rs294770	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs294775	0.82[EUR][1000 genomes]
rs294778	0.86[EUR][1000 genomes]
rs34100980	0.88[EUR][1000 genomes]
rs56068220	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57504651	0.97[EUR][1000 genomes]
rs58813047	0.97[EUR][1000 genomes]
rs61749966	0.86[EUR][1000 genomes]
rs61750900	0.86[EUR][1000 genomes]
rs6600854	0.86[EUR][1000 genomes]
rs6600855	0.86[EUR][1000 genomes]
rs6836520	0.84[EUR][1000 genomes]
rs72846859	0.93[EUR][1000 genomes]
rs72848040	0.97[EUR][1000 genomes]
rs72848056	0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7657958	0.86[EUR][1000 genomes]
rs7660491	0.82[EUR][1000 genomes]
rs7661050	0.86[EUR][1000 genomes]
rs7665996	0.86[EUR][1000 genomes]
rs7671312	0.88[EUR][1000 genomes]
rs7674919	0.86[EUR][1000 genomes]
rs7676146	0.86[EUR][1000 genomes]
rs7676529	0.84[EUR][1000 genomes]
rs7678526	0.82[EUR][1000 genomes]
rs7685333	0.86[EUR][1000 genomes]
rs7687951	0.86[EUR][1000 genomes]
rs7698940	0.86[EUR][1000 genomes]
rs835309	0.86[EUR][1000 genomes]
rs835315	0.86[EUR][1000 genomes]
rs835316	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs835317	0.86[EUR][1000 genomes]
rs844342	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs861340	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9993124	0.88[EUR][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	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv2763366	chr4:69592847-69661427	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1013885	chr4:69592847-69667996	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv829961	chr4:69592847-69695467	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv594579	chr4:69597175-69665970	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1014042	chr4:69599853-69667996	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv594580	chr4:69629425-69706273	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr4:69639000-69643200	Weak transcription	Fetal Intestine Large	intestine
2	chr4:69640000-69645200	Weak transcription	Fetal Intestine Small	intestine

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