Variant report

Variant	rs4719891
Chromosome Location	chr7:27430176-27430177
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10232941	0.85[ASN][1000 genomes]
rs10252971	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10268859	0.84[ASN][1000 genomes]
rs10951164	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs10951165	0.92[CHB][hapmap];0.84[ASN][1000 genomes]
rs11563380	0.92[CHB][hapmap];0.87[ASN][1000 genomes]
rs11563567	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs11978918	0.91[CHB][hapmap];0.87[ASN][1000 genomes]
rs12667419	0.85[ASN][1000 genomes]
rs12672272	0.84[ASN][1000 genomes]
rs17429361	0.83[CHB][hapmap]
rs17429641	0.92[CHB][hapmap];0.87[ASN][1000 genomes]
rs17429648	0.91[CHB][hapmap];0.87[ASN][1000 genomes]
rs17439000	0.83[CHB][hapmap]
rs17439221	0.92[CHB][hapmap];0.87[ASN][1000 genomes]
rs17439235	0.92[CHB][hapmap];0.87[ASN][1000 genomes]
rs17439374	0.83[ASN][1000 genomes]
rs2074336	0.87[ASN][1000 genomes]
rs2074337	0.89[AFR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2074338	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2893286	0.84[ASN][1000 genomes]
rs4298409	0.91[CHB][hapmap];0.87[ASN][1000 genomes]
rs4470906	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs4529360	0.84[ASN][1000 genomes]
rs58842477	0.81[ASN][1000 genomes]
rs6953463	0.88[AFR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6957441	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6957649	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7798437	0.89[AFR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs929242	0.92[CHB][hapmap];0.83[ASN][1000 genomes]
rs929243	0.88[ASN][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	nsv531024	chr7:27194426-27461954	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
2	nsv830930	chr7:27395838-27587355	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr7:27428000-27430200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:27428400-27430200	Enhancers	Fetal Muscle Leg	muscle
3	chr7:27428800-27430400	Enhancers	Adipose Nuclei	Adipose
4	chr7:27429800-27430200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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