Variant report

Variant	rs7013387
Chromosome Location	chr8:65757138-65757139
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10098783	1.00[CEU][hapmap];0.86[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10283033	1.00[CEU][hapmap];0.80[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11781142	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13271194	1.00[CEU][hapmap];0.80[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2356986	0.89[JPT][hapmap]
rs2884074	0.89[JPT][hapmap]
rs4236936	1.00[CEU][hapmap];0.80[CHB][hapmap];0.86[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4258041	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs4269577	1.00[CEU][hapmap];0.86[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4392942	1.00[CEU][hapmap];0.80[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4397440	1.00[MEX][hapmap]
rs4472561	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4527914	1.00[MEX][hapmap]
rs4549812	1.00[CEU][hapmap];0.86[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4737682	1.00[CEU][hapmap];0.90[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap]
rs6472149	1.00[ASW][hapmap];0.90[YRI][hapmap]
rs6472151	1.00[CEU][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6472152	1.00[CEU][hapmap];1.00[MEX][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6472154	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6987861	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs7814191	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7814895	0.86[AFR][1000 genomes]
rs7821085	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs7829301	1.00[CEU][hapmap];0.80[CHB][hapmap];0.90[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7842113	1.00[CEU][hapmap];0.80[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv534001	chr8:64992196-65798776	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	esv2761434	chr8:65578467-66567678	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65753000-65757400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:65754400-65757400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:65756200-65757400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:65756200-65757400	Weak transcription	NHDF-Ad	bronchial
5	chr8:65756400-65761200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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