Variant report

Variant	rs9474848
Chromosome Location	chr6:54274783-54274784
allele	C/T
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:48)

rs_ID	r²[population]
rs10484641	1.00[JPT][hapmap]
rs12055413	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12055863	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12175364	1.00[ASN][1000 genomes]
rs12176182	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12180097	1.00[EUR][1000 genomes]
rs16885263	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs2291824	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs3777637	1.00[EUR][1000 genomes]
rs3777638	1.00[EUR][1000 genomes]
rs3777639	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs3777641	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs3777642	1.00[JPT][hapmap]
rs60021603	1.00[EUR][1000 genomes]
rs73446702	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73448726	0.84[AFR][1000 genomes]
rs9349707	1.00[EUR][1000 genomes]
rs9357803	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9367564	1.00[JPT][hapmap]
rs9367565	1.00[JPT][hapmap]
rs9367567	1.00[EUR][1000 genomes]
rs9367571	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9370293	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9370294	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9370297	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9370298	0.95[ASN][1000 genomes]
rs9382324	1.00[JPT][hapmap]
rs9382327	1.00[EUR][1000 genomes]
rs9382328	1.00[EUR][1000 genomes]
rs9382339	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9382340	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395938	1.00[EUR][1000 genomes]
rs9395940	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs9395941	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs9395945	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs9395946	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs9395952	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9395955	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395956	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395957	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395960	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395961	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395963	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9474814	1.00[JPT][hapmap]
rs9474858	0.90[AFR][1000 genomes]
rs9474861	0.90[AFR][1000 genomes]
rs9474863	0.85[AFR][1000 genomes]
rs9474865	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[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	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr6:54269400-54284400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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