Variant report

Variant	rs57187918
Chromosome Location	chr8:91345523-91345524
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs55892713	1.00[AMR][1000 genomes]
rs56020750	1.00[AMR][1000 genomes]
rs56380820	1.00[AMR][1000 genomes]
rs56763575	1.00[AMR][1000 genomes]
rs57640703	1.00[AMR][1000 genomes]
rs60432986	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:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018991	chr8:91336887-91374274	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 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	chr8:91337000-91353200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:91344200-91345600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:91345000-91345600	ZNF genes & repeats	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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