Variant report

Variant	rs1390725
Chromosome Location	chr7:146963098-146963099
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]
rs10085456	0.89[JPT][hapmap]
rs10085764	1.00[JPT][hapmap]
rs1021008	0.81[CHD][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs10225100	1.00[JPT][hapmap]
rs10234386	1.00[JPT][hapmap]
rs10238730	1.00[JPT][hapmap]
rs10242430	1.00[JPT][hapmap]
rs10248220	0.91[JPT][hapmap]
rs10251412	1.00[JPT][hapmap]
rs10261539	0.81[JPT][hapmap]
rs10262107	1.00[JPT][hapmap]
rs10268597	1.00[JPT][hapmap]
rs10276382	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs10278315	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10279700	0.85[CHB][hapmap];0.91[CHD][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs10808044	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs10952678	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12531764	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs12534978	0.91[JPT][hapmap]
rs12538316	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs12703895	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12703900	1.00[JPT][hapmap]
rs13235260	0.91[JPT][hapmap]
rs1383011	0.91[JPT][hapmap]
rs1390724	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1404707	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs1496548	1.00[CEU][hapmap]
rs1496549	1.00[JPT][hapmap]
rs1525211	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1525215	0.80[CHD][hapmap];0.91[JPT][hapmap]
rs1525216	0.91[JPT][hapmap]
rs17170378	0.83[JPT][hapmap]
rs17170379	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs2132591	0.90[JPT][hapmap]
rs2620439	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs2692186	1.00[JPT][hapmap]
rs2692187	1.00[JPT][hapmap]
rs34748606	0.84[ASN][1000 genomes]
rs4637733	0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs4725708	1.00[JPT][hapmap]
rs4725709	0.83[CHD][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap]
rs4726833	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap]
rs4726834	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.80[TSI][hapmap]
rs4726835	1.00[JPT][hapmap]
rs66602672	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6962971	0.91[JPT][hapmap]
rs6974852	0.91[JPT][hapmap]
rs7790788	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs885610	0.82[JPT][hapmap]
rs9769600	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.86[TSI][hapmap]

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	nsv933033	chr7:146720301-147081560	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1033898	chr7:146721499-147081768	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv889395	chr7:146848251-146969389	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv889396	chr7:146854133-147035067	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr7:146961600-146963600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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