Variant report

Variant	rs6710046
Chromosome Location	chr2:37405655-37405656
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:10)

rs_ID	r²[population]
rs13022403	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3845786	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4670670	0.89[ASN][1000 genomes]
rs4670671	0.89[ASN][1000 genomes]
rs4670674	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6544059	0.80[EUR][1000 genomes]
rs6706672	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6734866	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6748151	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7583355	0.86[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37405200-37406400	Weak transcription	Primary neutrophils fromperipheralblood	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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