Variant report

Variant	rs4692482
Chromosome Location	chr4:30902325-30902326
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10001740	0.90[ASW][hapmap];0.82[LWK][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes]
rs10939323	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10939324	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12640768	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12641355	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs12641436	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12642486	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12643430	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12650559	0.92[JPT][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13101341	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13123980	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1374656	0.83[CHD][hapmap]
rs1447370	0.81[YRI][hapmap]
rs34280337	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34317883	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34347677	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35231537	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35427881	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35580687	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36048465	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4359861	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4386561	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4532197	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4692106	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4692108	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4692486	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5014904	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56829853	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs59134115	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs67044628	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67502847	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6816969	0.82[ASW][hapmap]
rs72619194	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72619195	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72619196	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72619197	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72619198	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72619199	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9884332	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878810	chr4:30823157-30987395	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30870800-30903200	Weak transcription	Fetal Lung	lung
2	chr4:30891600-30903400	Weak transcription	Fetal Kidney	kidney
3	chr4:30901400-30904600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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