Variant report

Variant	rs6829758
Chromosome Location	chr4:62686013-62686014
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10517548	1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11723129	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11724057	1.00[CEU][hapmap];0.83[GIH][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes]
rs11724143	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11724834	0.99[EUR][1000 genomes]
rs11725404	0.83[GIH][hapmap];0.81[TSI][hapmap]
rs11727239	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11732286	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11734361	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1450903	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1470722	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17226265	0.97[ASN][1000 genomes]
rs17292030	1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17292037	1.00[ASN][1000 genomes]
rs17292044	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1839617	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2015569	1.00[GIH][hapmap]
rs2345042	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs35113693	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35680649	0.91[ASN][1000 genomes]
rs57991081	0.94[ASN][1000 genomes]
rs58739264	0.97[ASN][1000 genomes]
rs60536298	0.98[ASN][1000 genomes]
rs60683749	0.92[ASN][1000 genomes]
rs6551657	1.00[CEU][hapmap];0.83[GIH][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes]
rs6551661	0.83[JPT][hapmap]
rs6814909	0.97[ASN][1000 genomes]
rs6815347	0.83[GIH][hapmap]
rs6824026	1.00[ASN][1000 genomes]
rs6839737	0.97[ASN][1000 genomes]
rs6839996	0.97[ASN][1000 genomes]
rs6840216	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs6842293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6846860	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs73823242	0.97[ASN][1000 genomes]
rs73823243	0.94[ASN][1000 genomes]
rs73823248	0.97[ASN][1000 genomes]
rs73823249	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73823250	0.92[ASN][1000 genomes]
rs7654504	1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7657806	0.92[ASN][1000 genomes]
rs7662566	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7667328	0.83[GIH][hapmap]
rs7671445	0.97[ASN][1000 genomes]
rs7671478	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7676199	1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7683391	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7689173	0.85[EUR][1000 genomes]
rs7690254	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7694929	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7697485	0.90[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7698778	1.00[JPT][hapmap];0.92[ASN][1000 genomes]

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	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv829949	chr4:62615637-62761629	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428760	chr4:62649399-62824542	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62681200-62693000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:62682600-62697600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:62682800-62686200	Weak transcription	Aorta	Aorta
4	chr4:62683400-62689400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:62683400-62697400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:62683600-62686400	Weak transcription	Fetal Kidney	kidney
7	chr4:62684000-62686400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr4:62685800-62686600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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