Variant report

Variant	rs73553716
Chromosome Location	chr6:132547567-132547568
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs59647867	1.00[EUR][1000 genomes]
rs60774416	1.00[EUR][1000 genomes]
rs73549533	1.00[EUR][1000 genomes]
rs73549567	1.00[EUR][1000 genomes]
rs73549592	1.00[EUR][1000 genomes]
rs73551714	1.00[EUR][1000 genomes]
rs73551722	1.00[EUR][1000 genomes]
rs73551732	1.00[EUR][1000 genomes]
rs73551740	1.00[EUR][1000 genomes]
rs73551766	1.00[EUR][1000 genomes]
rs73551794	1.00[EUR][1000 genomes]
rs73551802	1.00[EUR][1000 genomes]
rs73553722	1.00[EUR][1000 genomes]
rs7741927	1.00[EUR][1000 genomes]
rs7750378	1.00[EUR][1000 genomes]
rs7771183	1.00[EUR][1000 genomes]
rs7771622	1.00[EUR][1000 genomes]
rs9483373	1.00[EUR][1000 genomes]
rs9483375	1.00[EUR][1000 genomes]
rs9493168	1.00[EUR][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	esv2762616	chr6:132404708-132584324	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1024527	chr6:132532941-132571889	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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