Variant report

Variant	rs61960379
Chromosome Location	chr13:50438964-50438965
allele	C/T
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:10)

rs_ID	r²[population]
rs55813792	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55825121	0.86[EUR][1000 genomes]
rs56079328	0.92[EUR][1000 genomes]
rs61960374	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61960375	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61961517	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7320514	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7322027	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7322028	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7986486	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50434200-50442000	Weak transcription	Pancreas	Pancrea

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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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