Variant report

Variant	rs7757433
Chromosome Location	chr6:54309630-54309631
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10807471	0.87[EUR][1000 genomes]
rs10807472	0.87[EUR][1000 genomes]
rs12055676	0.87[EUR][1000 genomes]
rs1477583	0.87[EUR][1000 genomes]
rs171492	0.83[ASN][1000 genomes]
rs1820408	0.87[EUR][1000 genomes]
rs1834483	0.87[EUR][1000 genomes]
rs243772	0.82[ASN][1000 genomes]
rs243773	0.82[ASN][1000 genomes]
rs243801	0.86[ASN][1000 genomes]
rs243816	0.83[ASN][1000 genomes]
rs243818	0.81[ASN][1000 genomes]
rs3864316	0.87[EUR][1000 genomes]
rs4090740	0.87[EUR][1000 genomes]
rs4280961	0.87[EUR][1000 genomes]
rs4427000	0.87[EUR][1000 genomes]
rs496285	0.97[EUR][1000 genomes]
rs513780	0.97[EUR][1000 genomes]
rs515020	0.83[ASN][1000 genomes]
rs519386	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs522159	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs530355	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs558698	0.97[EUR][1000 genomes]
rs564704	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs569189	0.97[EUR][1000 genomes]
rs57572567	0.87[EUR][1000 genomes]
rs587128	0.97[EUR][1000 genomes]
rs59094137	0.87[EUR][1000 genomes]
rs615537	0.92[EUR][1000 genomes]
rs634239	0.97[EUR][1000 genomes]
rs638540	0.82[ASN][1000 genomes]
rs661622	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs675064	0.97[EUR][1000 genomes]
rs7742798	0.87[EUR][1000 genomes]
rs9349714	0.87[EUR][1000 genomes]
rs9349716	0.87[EUR][1000 genomes]
rs9357809	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9367576	0.87[EUR][1000 genomes]
rs9367577	0.87[EUR][1000 genomes]
rs9367578	0.87[EUR][1000 genomes]
rs9370303	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs9370304	0.87[EUR][1000 genomes]
rs9370308	0.87[EUR][1000 genomes]
rs9370311	0.87[EUR][1000 genomes]
rs9382350	0.87[EUR][1000 genomes]
rs9382352	0.81[EUR][1000 genomes]
rs9382354	0.87[EUR][1000 genomes]
rs9382355	0.87[EUR][1000 genomes]
rs9382356	0.87[EUR][1000 genomes]
rs9395966	0.87[EUR][1000 genomes]
rs9395968	0.82[EUR][1000 genomes]
rs9395973	0.87[EUR][1000 genomes]
rs9474894	0.87[EUR][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	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
3	nsv528901	chr6:54290333-54337130	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv427757	chr6:54296552-54507210	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr6:54309600-54310200	Enhancers	Osteobl	bone

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