Variant report

Variant	rs2947350
Chromosome Location	chr2:58071224-58071225
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10445894	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10496078	0.82[ASN][1000 genomes]
rs10496079	0.81[ASN][1000 genomes]
rs10865304	0.83[ASN][1000 genomes]
rs1106090	0.81[CEU][hapmap]
rs1106302	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11684106	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11898858	0.84[ASN][1000 genomes]
rs12713358	0.84[ASN][1000 genomes]
rs12990792	0.82[ASN][1000 genomes]
rs12997222	0.82[ASN][1000 genomes]
rs1402398	0.86[ASN][1000 genomes]
rs1568450	0.83[ASN][1000 genomes]
rs1589407	0.83[ASN][1000 genomes]
rs2090793	0.82[ASN][1000 genomes]
rs2176931	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2204019	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2683614	0.83[ASN][1000 genomes]
rs2683616	0.86[ASN][1000 genomes]
rs2683619	0.85[ASN][1000 genomes]
rs2683620	0.85[ASN][1000 genomes]
rs2683622	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2683625	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2683628	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2683629	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2716998	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2716999	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2717018	0.86[ASN][1000 genomes]
rs2717048	0.83[ASN][1000 genomes]
rs2717070	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2717072	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2717075	0.85[ASN][1000 genomes]
rs2947351	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2953437	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2953438	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2953439	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2953441	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2953443	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4672223	0.82[ASN][1000 genomes]
rs6545663	0.82[ASN][1000 genomes]
rs6545664	0.82[ASN][1000 genomes]
rs6545665	0.82[ASN][1000 genomes]
rs66985942	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6730037	0.84[ASN][1000 genomes]
rs6737913	0.85[ASN][1000 genomes]
rs6756221	0.84[ASN][1000 genomes]
rs6761347	0.85[ASN][1000 genomes]
rs7561842	0.82[ASN][1000 genomes]
rs7588492	0.81[ASN][1000 genomes]
rs7598169	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007118	chr2:57562051-58147588	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv874196	chr2:57946148-58220320	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv834148	chr2:57979661-58119213	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1010981	chr2:58013389-58205699	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv874199	chr2:58031249-58161520	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:58070600-58073400	Weak transcription	Pancreas	Pancrea

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