Variant report

Variant	rs11722451
Chromosome Location	chr4:69669603-69669604
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10000284	0.91[EUR][1000 genomes]
rs10010381	0.91[EUR][1000 genomes]
rs10010497	0.91[EUR][1000 genomes]
rs10028938	0.97[EUR][1000 genomes]
rs11724821	0.87[EUR][1000 genomes]
rs11725000	0.89[EUR][1000 genomes]
rs11725119	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11725502	0.94[EUR][1000 genomes]
rs11726045	0.88[EUR][1000 genomes]
rs11731269	0.93[EUR][1000 genomes]
rs11734565	0.94[EUR][1000 genomes]
rs11735873	0.86[EUR][1000 genomes]
rs11736654	0.89[EUR][1000 genomes]
rs11737527	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11737644	0.96[EUR][1000 genomes]
rs11737672	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1902932	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2175776	0.89[EUR][1000 genomes]
rs2331437	0.89[EUR][1000 genomes]
rs2331438	0.89[EUR][1000 genomes]
rs2331439	0.89[EUR][1000 genomes]
rs2331559	0.92[EUR][1000 genomes]
rs2926036	0.84[EUR][1000 genomes]
rs2926038	0.89[EUR][1000 genomes]
rs2942856	0.89[EUR][1000 genomes]
rs294759	0.92[EUR][1000 genomes]
rs294770	0.92[EUR][1000 genomes]
rs294775	0.93[EUR][1000 genomes]
rs294778	0.97[EUR][1000 genomes]
rs34100980	1.00[EUR][1000 genomes]
rs56068220	0.91[EUR][1000 genomes]
rs57504651	0.91[EUR][1000 genomes]
rs58813047	0.91[EUR][1000 genomes]
rs61749966	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61750900	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6600854	0.87[EUR][1000 genomes]
rs6600855	0.87[EUR][1000 genomes]
rs6815399	0.87[EUR][1000 genomes]
rs6830149	0.86[EUR][1000 genomes]
rs6836520	0.96[EUR][1000 genomes]
rs72846859	0.94[EUR][1000 genomes]
rs72848040	0.88[EUR][1000 genomes]
rs72848056	0.89[EUR][1000 genomes]
rs7657958	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7658577	0.86[EUR][1000 genomes]
rs7660491	0.93[EUR][1000 genomes]
rs7661050	0.87[EUR][1000 genomes]
rs7665996	0.87[EUR][1000 genomes]
rs7671312	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7674919	0.87[EUR][1000 genomes]
rs7676146	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7676529	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7678526	0.82[EUR][1000 genomes]
rs7685333	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7687748	0.89[EUR][1000 genomes]
rs7687951	0.87[EUR][1000 genomes]
rs7698940	0.87[EUR][1000 genomes]
rs835309	0.97[EUR][1000 genomes]
rs835315	0.97[EUR][1000 genomes]
rs835316	0.89[EUR][1000 genomes]
rs835317	0.97[EUR][1000 genomes]
rs844342	0.84[EUR][1000 genomes]
rs861340	0.85[EUR][1000 genomes]
rs9329034	0.88[EUR][1000 genomes]
rs9993124	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
3	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
4	nsv999654	chr4:69661415-70132110	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
5	nsv879377	chr4:69663003-69771935	Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1005777	chr4:69665571-69713817	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv869970	chr4:69665769-69713522	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1007851	chr4:69667996-69713817	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv2760902	chr4:69668008-69723767	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:69668400-69670000	Enhancers	Fetal Intestine Small	intestine
2	chr4:69669400-69673000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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