Variant report

Variant	rs815715
Chromosome Location	chr3:61264084-61264085
allele	C/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:50)

rs_ID	r²[population]
rs10866046	0.85[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs11130821	0.82[CHB][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes]
rs11130822	0.82[EUR][1000 genomes]
rs11130826	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11130833	0.82[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs11130834	0.85[ASN][1000 genomes]
rs11130835	0.84[ASN][1000 genomes]
rs11720254	0.81[EUR][1000 genomes]
rs12492551	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1470035	0.81[JPT][hapmap]
rs1524019	0.96[CEU][hapmap];0.91[EUR][1000 genomes]
rs1554599	0.84[CHB][hapmap];0.89[JPT][hapmap];0.83[EUR][1000 genomes]
rs17064630	0.82[EUR][1000 genomes]
rs1916800	0.85[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes]
rs1916801	0.82[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes]
rs1916802	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs1949772	0.90[EUR][1000 genomes]
rs1980308	0.86[CHB][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes]
rs1980309	0.86[CHB][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes]
rs1980310	0.86[CHB][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes]
rs1980311	0.82[EUR][1000 genomes]
rs2365389	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs35198002	0.82[EUR][1000 genomes]
rs4296587	0.87[EUR][1000 genomes]
rs4535219	0.87[CEU][hapmap];0.81[EUR][1000 genomes]
rs4605537	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4688352	0.81[EUR][1000 genomes]
rs4688354	0.80[EUR][1000 genomes]
rs4688355	0.81[EUR][1000 genomes]
rs4688379	0.83[EUR][1000 genomes]
rs6445197	0.87[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6445198	0.86[CHB][hapmap];0.91[JPT][hapmap];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6445199	0.87[EUR][1000 genomes]
rs6445200	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs6785875	0.91[EUR][1000 genomes]
rs6787292	0.86[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes]
rs6809031	0.88[EUR][1000 genomes]
rs71296711	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs815709	0.93[EUR][1000 genomes]
rs815710	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs815712	0.92[EUR][1000 genomes]
rs815717	0.93[EUR][1000 genomes]
rs843812	0.91[EUR][1000 genomes]
rs863635	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9831249	0.90[EUR][1000 genomes]
rs9844741	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs9846073	0.85[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes]
rs9850114	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9855716	0.96[CEU][hapmap];0.91[EUR][1000 genomes]
rs9859004	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876866	chr3:61054494-61310328	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv876867	chr3:61054494-61474575	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv432423	chr3:61100255-61606060	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv876868	chr3:61145050-61282503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv532626	chr3:61159646-61388418	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1008399	chr3:61176965-61461349	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv998982	chr3:61252469-61364001	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 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	chr3:61261800-61269600	Weak transcription	Aorta	Aorta
2	chr3:61262000-61264200	Enhancers	GM12878-XiMat	blood

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