Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11723129	0.85[EUR][1000 genomes]
rs11724057	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11724834	0.84[EUR][1000 genomes]
rs11725404	1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11727239	0.85[EUR][1000 genomes]
rs11732286	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11734361	0.85[EUR][1000 genomes]
rs1450903	1.00[CEU][hapmap]
rs1839617	0.85[EUR][1000 genomes]
rs35113693	0.85[EUR][1000 genomes]
rs6551657	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6815347	1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6829758	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs6840216	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6842293	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs6848408	0.82[YRI][hapmap]
rs73823249	0.84[EUR][1000 genomes]
rs7662566	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7671478	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7683391	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7689173	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7690254	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7694929	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7697485	0.90[CEU][hapmap];0.83[EUR][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	chr4:62683400-62689400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:62683400-62697400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:62686200-62686800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:62686400-62686800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr4:62686400-62687000	Enhancers	Fetal Kidney	kidney
8	chr4:62686600-62693200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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