Variant report

Variant	rs13166524
Chromosome Location	chr5:57884481-57884482
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10070522	0.83[ASN][1000 genomes]
rs10070704	0.95[ASN][1000 genomes]
rs1508908	0.83[ASN][1000 genomes]
rs1559240	0.82[ASN][1000 genomes]
rs2029690	0.82[ASN][1000 genomes]
rs6450481	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6862791	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6866818	0.95[ASN][1000 genomes]
rs6894735	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57881000-57885400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:57882600-57885600	Weak transcription	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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