Variant report

Variant	rs60432986
Chromosome Location	chr8:91415061-91415062
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs55892713	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56020750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56380820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56763575	1.00[AMR][1000 genomes]
rs57187918	1.00[AMR][1000 genomes]
rs57640703	1.00[AMR][1000 genomes]
rs73297284	1.00[AMR][1000 genomes]
rs73297296	1.00[AMR][1000 genomes]
rs73695388	1.00[AMR][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	esv3525740	chr8:91410176-91416274	Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3525742	chr8:91410176-91416274	Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91395000-91433400	Weak transcription	K562	blood

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Input of quick search could be:

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

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