Variant report

Variant	rs2463311
Chromosome Location	chr6:114063457-114063458
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11153440	0.83[ASN][1000 genomes]
rs11153450	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs12204831	0.83[ASN][1000 genomes]
rs1980375	0.90[CHB][hapmap]
rs1997216	0.83[ASN][1000 genomes]
rs2498753	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2498754	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6919507	0.81[CHB][hapmap]
rs6928789	0.82[ASN][1000 genomes]
rs7764889	0.82[ASN][1000 genomes]
rs9372377	0.83[ASN][1000 genomes]
rs9372379	0.90[CHB][hapmap]
rs9384883	0.83[ASN][1000 genomes]
rs9400664	0.81[AMR][1000 genomes]
rs9400665	0.81[AMR][1000 genomes]
rs9481393	0.82[ASN][1000 genomes]
rs954620	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114062800-114064200	Enhancers	Fetal Heart	heart
2	chr6:114063200-114064000	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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