Variant report

Variant	rs1447617
Chromosome Location	chr3:160610280-160610281
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10513558	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs11709802	1.00[CEU][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes]
rs12485723	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12496196	0.92[CEU][hapmap]
rs12498008	1.00[CEU][hapmap]
rs12635022	0.84[EUR][1000 genomes]
rs12696110	0.92[JPT][hapmap]
rs13079358	0.90[CEU][hapmap]
rs13079792	0.84[EUR][1000 genomes]
rs13086445	0.87[EUR][1000 genomes]
rs1348977	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1447616	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1447624	0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1562466	1.00[CEU][hapmap]
rs16831758	1.00[CEU][hapmap]
rs1839014	0.86[ASN][1000 genomes]
rs1839020	0.87[EUR][1000 genomes]
rs1868104	1.00[CEU][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes]
rs1868106	0.92[JPT][hapmap]
rs1971240	1.00[CEU][hapmap]
rs2028988	1.00[CEU][hapmap];0.83[JPT][hapmap]
rs4679667	1.00[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.90[EUR][1000 genomes]
rs4679925	0.84[EUR][1000 genomes]
rs6441333	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6441334	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6441335	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6441336	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6441342	0.87[EUR][1000 genomes]
rs6441343	0.84[EUR][1000 genomes]
rs6441344	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs6770488	0.93[JPT][hapmap]
rs6776120	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6785844	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6787694	1.00[CEU][hapmap]
rs6789195	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6797498	0.84[JPT][hapmap];0.82[EUR][1000 genomes]
rs6799391	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7610732	1.00[CEU][hapmap];0.84[JPT][hapmap];0.83[EUR][1000 genomes]
rs7617759	0.91[CEU][hapmap]
rs7619552	0.82[EUR][1000 genomes]
rs7629001	0.82[EUR][1000 genomes]
rs7629374	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7636886	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7653744	0.82[EUR][1000 genomes]
rs778647	1.00[CEU][hapmap]
rs778650	0.84[CEU][hapmap]
rs796610	1.00[CEU][hapmap]
rs878954	0.85[EUR][1000 genomes]
rs878955	0.84[EUR][1000 genomes]
rs935496	0.93[EUR][1000 genomes]
rs935500	0.87[EUR][1000 genomes]
rs9814174	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9818081	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv1009249	chr3:160496237-160627378	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv536780	chr3:160496237-160627378	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv3391648	chr3:160602299-160620598	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160604400-160616600	Weak transcription	Psoas Muscle	Psoas
2	chr3:160610000-160611400	Enhancers	Primary neutrophils fromperipheralblood	blood

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