Variant report

Variant	rs7257941
Chromosome Location	chr19:40216293-40216294
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10421474	0.93[ASN][1000 genomes]
rs11083535	0.88[ASN][1000 genomes]
rs11666142	0.88[ASN][1000 genomes]
rs11666190	0.88[ASN][1000 genomes]
rs11666517	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11669501	0.88[ASN][1000 genomes]
rs11669658	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11670568	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11878990	0.87[ASN][1000 genomes]
rs11879130	0.87[ASN][1000 genomes]
rs11881937	0.81[ASN][1000 genomes]
rs11883181	0.88[ASN][1000 genomes]
rs12609196	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12610197	0.88[ASN][1000 genomes]
rs12610386	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12610398	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12610904	0.88[ASN][1000 genomes]
rs12610934	0.81[ASN][1000 genomes]
rs12611052	0.87[ASN][1000 genomes]
rs12611097	0.87[ASN][1000 genomes]
rs12611334	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16973570	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17641958	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17709242	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1985359	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2286757	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2355335	0.93[ASN][1000 genomes]
rs28816119	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35332571	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3810387	0.81[ASN][1000 genomes]
rs3810388	0.81[ASN][1000 genomes]
rs3810389	0.81[ASN][1000 genomes]
rs3810392	0.81[ASN][1000 genomes]
rs3810396	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3826923	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs386545	0.97[ASN][1000 genomes]
rs3922304	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4141230	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4141231	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4629090	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55678764	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55850506	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56205202	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56243473	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56261485	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56346568	0.87[EUR][1000 genomes]
rs56400901	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57145045	0.81[ASN][1000 genomes]
rs58920360	0.81[ASN][1000 genomes]
rs59097080	0.88[ASN][1000 genomes]
rs60928622	0.81[ASN][1000 genomes]
rs61208282	0.87[ASN][1000 genomes]
rs62121666	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62121667	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62121738	0.89[ASN][1000 genomes]
rs62121739	0.87[ASN][1000 genomes]
rs62121741	0.88[ASN][1000 genomes]
rs62121742	0.88[ASN][1000 genomes]
rs62121748	0.87[ASN][1000 genomes]
rs62121749	0.87[ASN][1000 genomes]
rs62121750	0.82[ASN][1000 genomes]
rs62121753	0.81[ASN][1000 genomes]
rs62121754	0.81[ASN][1000 genomes]
rs62121755	0.81[ASN][1000 genomes]
rs62121756	0.81[ASN][1000 genomes]
rs62123700	0.81[ASN][1000 genomes]
rs6508902	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6508905	0.87[ASN][1000 genomes]
rs718798	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs718799	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7248546	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73036596	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73036598	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7507315	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8100721	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8106628	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8109921	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8110945	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8112007	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs978671	0.87[ASN][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	nsv1057361	chr19:40123868-40310996	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1061361	chr19:40131820-40310996	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv579511	chr19:40132825-40310497	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1062394	chr19:40133229-40310186	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv544004	chr19:40133229-40310186	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1059691	chr19:40168862-40306373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv544005	chr19:40168862-40306373	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	esv3332670	chr19:40181720-40297955	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	esv3329492	chr19:40198535-40437035	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 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	chr19:40201600-40216800	Weak transcription	Placenta	Placenta
2	chr19:40213000-40216600	Weak transcription	GM12878-XiMat	blood

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