Variant report

Variant	rs4279396
Chromosome Location	chr6:74786415-74786416
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10485388	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11751061	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11751175	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11751771	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11754164	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11756254	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11757198	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12190509	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12191462	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12191866	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12193999	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12198091	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12202104	0.89[EUR][1000 genomes]
rs12202674	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12205582	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12205749	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12206043	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12209564	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12209571	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12213297	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12215639	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3923228	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4537105	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4546447	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4644011	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55789428	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56104278	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56138029	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56362119	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56396434	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs66472340	0.91[EUR][1000 genomes]
rs66865230	0.91[EUR][1000 genomes]
rs72952371	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72952395	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72952398	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72955171	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72955173	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72955185	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72955196	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72955199	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72955201	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72962230	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030389	chr6:74606701-74811706	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3394316	chr6:74630005-74935625	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv603733	chr6:74666559-74944460	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3327625	chr6:74716120-74971605	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv3440413	chr6:74741688-74791357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv886161	chr6:74765488-74800529	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1017333	chr6:74776830-74907758	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv538307	chr6:74776830-74907758	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74784200-74786600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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