Variant report

Variant	rs60899707
Chromosome Location	chr5:91766640-91766641
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs4351181	1.00[EUR][1000 genomes]
rs4485908	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60047729	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73129459	1.00[AMR][1000 genomes]
rs73129478	1.00[AMR][1000 genomes]
rs73131588	1.00[EUR][1000 genomes]
rs73131595	1.00[AMR][1000 genomes]
rs73133057	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73133062	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73133075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73133077	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73133079	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73134921	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73134929	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73134939	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763469	chr5:91759081-91812497	Enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	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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