Variant report

Variant	rs970766
Chromosome Location	chr4:167439985-167439986
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10007851	0.88[AMR][1000 genomes]
rs10008481	0.85[AMR][1000 genomes]
rs10010173	0.85[AMR][1000 genomes]
rs10019331	0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10020655	0.85[AMR][1000 genomes]
rs10025831	0.88[AMR][1000 genomes]
rs10026453	0.88[AMR][1000 genomes]
rs10857381	0.86[AMR][1000 genomes]
rs10857383	0.86[AMR][1000 genomes]
rs11100652	0.80[AMR][1000 genomes]
rs11100654	0.86[AMR][1000 genomes]
rs1160586	0.85[AMR][1000 genomes]
rs1160587	0.87[AMR][1000 genomes]
rs12499088	0.80[AMR][1000 genomes]
rs12501140	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12503120	0.80[AMR][1000 genomes]
rs12504728	0.88[AMR][1000 genomes]
rs12641852	0.85[AMR][1000 genomes]
rs1388885	0.85[AMR][1000 genomes]
rs1388886	0.89[AMR][1000 genomes]
rs1388887	0.86[AMR][1000 genomes]
rs1388888	0.85[AMR][1000 genomes]
rs1388889	0.86[AMR][1000 genomes]
rs17518913	0.85[AMR][1000 genomes]
rs17597276	0.85[AMR][1000 genomes]
rs1988968	0.85[AMR][1000 genomes]
rs2029641	0.92[EUR][1000 genomes]
rs2172319	0.85[AMR][1000 genomes]
rs28494733	0.85[AMR][1000 genomes]
rs28689804	0.85[AMR][1000 genomes]
rs28691004	0.85[AMR][1000 genomes]
rs28691761	0.85[AMR][1000 genomes]
rs4234899	0.86[AMR][1000 genomes]
rs4234900	0.86[AMR][1000 genomes]
rs4488904	0.86[AMR][1000 genomes]
rs4560359	0.87[AMR][1000 genomes]
rs4690848	0.85[AMR][1000 genomes]
rs4690849	0.86[AMR][1000 genomes]
rs4690850	0.85[AMR][1000 genomes]
rs4691288	0.86[AMR][1000 genomes]
rs4691289	0.86[AMR][1000 genomes]
rs72695503	0.87[AMR][1000 genomes]
rs72695514	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7662181	0.87[AMR][1000 genomes]
rs992020	0.88[AMR][1000 genomes]
rs992021	0.88[AMR][1000 genomes]
rs992022	0.90[AMR][1000 genomes]
rs9995641	0.85[AMR][1000 genomes]
rs9996713	0.86[AMR][1000 genomes]
rs9998119	0.81[AMR][1000 genomes]
rs9998923	0.83[AMR][1000 genomes]
rs9999260	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034421	chr4:166961339-167893289	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv537339	chr4:166961339-167893289	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv881405	chr4:167193885-167628013	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1023051	chr4:167304814-168211540	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv537340	chr4:167304814-168211540	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv881309	chr4:167377133-167500233	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv830143	chr4:167386232-167538014	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1017028	chr4:167420519-167697787	Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr4:167439400-167440800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:167439400-167441400	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr4:167439600-167440800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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