Variant report

Variant	rs7795946
Chromosome Location	chr7:137785091-137785092
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10228366	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10228704	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10244249	0.90[ASN][1000 genomes]
rs10244250	0.90[ASN][1000 genomes]
rs10246884	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs1025967	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10263205	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10264658	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10274304	0.90[ASN][1000 genomes]
rs10280394	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10280628	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1038626	0.84[ASN][1000 genomes]
rs10954602	0.91[CEU][hapmap];0.83[YRI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10954603	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11982192	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13243992	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1872929	0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1872930	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2035647	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2120846	0.90[CEU][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2166188	0.90[CEU][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2306847	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2859828	0.90[CEU][hapmap];0.91[EUR][1000 genomes]
rs3757393	0.86[CEU][hapmap];0.92[EUR][1000 genomes]
rs3805360	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3805361	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3807332	0.90[CEU][hapmap];0.92[EUR][1000 genomes]
rs3816829	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3857868	0.83[ASN][1000 genomes]
rs4732285	0.89[CEU][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6945659	0.90[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6977075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6980334	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7780066	0.89[ASN][1000 genomes]
rs7784881	0.90[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7787591	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9642091	0.81[ASN][1000 genomes]
rs9642092	0.83[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	nsv518070	chr7:137534627-137808839	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv831151	chr7:137711447-137865471	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137776600-137790000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:137782800-137802400	Strong transcription	Liver	Liver
3	chr7:137785000-137795800	Weak transcription	HepG2	liver

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