Variant report

Variant	rs13216585
Chromosome Location	chr6:11980411-11980412
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12525800	0.81[JPT][hapmap]
rs12530006	1.00[CEU][hapmap];0.90[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13213752	0.81[ASN][1000 genomes]
rs13362603	1.00[YRI][hapmap]
rs1475357	0.86[ASN][1000 genomes]
rs1475358	0.86[ASN][1000 genomes]
rs17676598	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2148254	0.86[ASN][1000 genomes]
rs2327509	0.85[YRI][hapmap]
rs4714081	0.88[ASN][1000 genomes]
rs6938400	0.89[CEU][hapmap]
rs9462364	0.86[ASN][1000 genomes]
rs9462377	1.00[YRI][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11979200-11983600	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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