Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10134176	1.00[CEU][hapmap];0.89[YRI][hapmap]
rs10136314	1.00[CEU][hapmap];0.87[YRI][hapmap]
rs10147103	1.00[CEU][hapmap];0.90[YRI][hapmap]
rs10873166	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11158471	0.95[CEU][hapmap];0.81[CHB][hapmap]
rs1950983	0.89[YRI][hapmap]
rs1950985	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[YRI][hapmap]
rs1956670	0.82[CHB][hapmap]
rs2356101	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs3850312	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs3915801	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4127780	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4584750	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs6573480	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs7141839	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs7156008	0.84[JPT][hapmap]
rs7159344	1.00[CEU][hapmap]
rs8006668	1.00[CEU][hapmap]
rs8015817	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs8017368	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs8019140	0.86[YRI][hapmap]
rs8020935	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs941709	0.82[CHB][hapmap]

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	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 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	chr14:63521600-63523200	Enhancers	Fetal Brain Male	brain

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