Variant report

Variant	rs73773521
Chromosome Location	chr6:133402935-133402936
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11963825	0.87[ASN][1000 genomes]
rs11965251	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs11965334	0.89[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4076846	0.95[ASN][1000 genomes]
rs4458711	0.95[ASN][1000 genomes]
rs4569980	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs5010276	0.91[ASN][1000 genomes]
rs5020765	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs56026451	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs56235131	0.91[ASN][1000 genomes]
rs57161904	0.91[ASN][1000 genomes]
rs57261444	0.91[ASN][1000 genomes]
rs57940911	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs58175086	0.95[ASN][1000 genomes]
rs58190426	0.91[ASN][1000 genomes]
rs58336680	0.95[ASN][1000 genomes]
rs58519358	0.91[ASN][1000 genomes]
rs59430285	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs60000557	0.91[ASN][1000 genomes]
rs60082145	0.91[ASN][1000 genomes]
rs60484160	0.91[ASN][1000 genomes]
rs60576607	0.91[ASN][1000 genomes]
rs60622734	0.91[ASN][1000 genomes]
rs60804293	0.91[ASN][1000 genomes]
rs61006452	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs61244591	0.91[ASN][1000 genomes]
rs61362264	0.91[ASN][1000 genomes]
rs61555922	0.91[ASN][1000 genomes]
rs73551650	0.89[EUR][1000 genomes]
rs73553617	0.91[ASN][1000 genomes]
rs73773507	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs73773508	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs73773509	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs73773520	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73773523	0.91[ASN][1000 genomes]
rs7741419	0.89[EUR][1000 genomes]
rs7747170	0.91[ASN][1000 genomes]
rs7752764	0.89[EUR][1000 genomes]
rs9493506	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv428154	chr6:133271975-133522803	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv3445931	chr6:133347824-133434532	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv519475	chr6:133350936-133474673	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 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	chr6:133402400-133403000	Enhancers	A549	lung
2	chr6:133402600-133403000	Enhancers	Fetal Lung	lung
3	chr6:133402800-133404400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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