Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12591677	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12592417	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12592614	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12595182	0.83[ASN][1000 genomes]
rs1807013	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28483579	0.97[ASN][1000 genomes]
rs35470430	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4886459	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4886460	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4886730	1.00[EUR][1000 genomes]
rs4886734	0.86[CHD][hapmap];1.00[JPT][hapmap]
rs4886737	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57596965	1.00[ASN][1000 genomes]
rs58189617	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59416499	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59737067	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61754538	1.00[EUR][1000 genomes]
rs7167845	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73441010	1.00[EUR][1000 genomes]
rs8028183	1.00[EUR][1000 genomes]
rs8033539	0.90[ASN][1000 genomes]
rs9744031	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531903	chr15:75889302-76342128	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv527186	chr15:75924443-76107730	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
3	nsv974599	chr15:76033068-76101142	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76068600-76075200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:76071000-76072600	Weak transcription	HepG2	liver
3	chr15:76071800-76072200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:76071800-76072600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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