Variant report

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

rs_ID	r²[population]
rs10004534	0.92[ASN][1000 genomes]
rs10020688	0.89[ASN][1000 genomes]
rs10213085	0.88[ASN][1000 genomes]
rs10471163	0.87[ASN][1000 genomes]
rs10520290	0.95[ASN][1000 genomes]
rs11725853	0.96[ASN][1000 genomes]
rs11737591	0.87[ASN][1000 genomes]
rs12509326	0.89[ASN][1000 genomes]
rs13142152	0.87[ASN][1000 genomes]
rs1586339	0.87[ASN][1000 genomes]
rs17060785	0.95[ASN][1000 genomes]
rs28408827	0.87[ASN][1000 genomes]
rs28432255	0.86[ASN][1000 genomes]
rs28538678	0.92[ASN][1000 genomes]
rs28688380	0.94[ASN][1000 genomes]
rs2877828	0.95[ASN][1000 genomes]
rs35706713	0.89[ASN][1000 genomes]
rs4447833	0.95[ASN][1000 genomes]
rs4594702	0.98[ASN][1000 genomes]
rs6853281	0.87[ASN][1000 genomes]
rs7656851	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7658547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7685854	0.98[ASN][1000 genomes]
rs9884969	0.88[ASN][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	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv880584	chr4:175505749-175644689	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175635000-175638400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr4:175635200-175638800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:175635400-175638600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:175635400-175638800	Weak transcription	Colon Smooth Muscle	Colon
5	chr4:175635600-175638600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:175638000-175638400	Weak transcription	Rectal Smooth Muscle	rectum

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