Variant report

Variant	rs2044613
Chromosome Location	chr3:60908013-60908014
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11714964	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11924304	0.96[CEU][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13094263	0.84[EUR][1000 genomes]
rs1349031	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1447918	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs1868220	0.93[ASW][hapmap];0.84[LWK][hapmap];0.86[MKK][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes]
rs1868225	0.96[CEU][hapmap];0.95[GIH][hapmap];0.97[LWK][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1868226	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1868227	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1868228	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2044611	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4974250	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4974251	0.92[CEU][hapmap];0.91[GIH][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56078561	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6446164	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6446165	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6789015	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6791911	1.00[CEU][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6793737	0.93[ASW][hapmap];0.84[LWK][hapmap];0.83[MKK][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes]
rs6799902	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7622539	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7631028	0.92[CEU][hapmap]
rs7636450	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7637834	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7645482	1.00[CEU][hapmap];0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7646138	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7652906	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9311788	0.87[YRI][hapmap];0.86[AFR][1000 genomes]
rs9754838	0.86[ASW][hapmap];0.96[CEU][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9757313	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9819076	0.96[CEU][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9827976	0.96[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9852553	0.86[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9854653	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs9857057	0.86[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9859690	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs9867960	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9876711	0.96[CEU][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9876863	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9990051	0.92[CEU][hapmap];0.98[GIH][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534038	chr3:60781917-60993082	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2757872	chr3:60781943-61019003	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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