Variant report

Variant	rs11128179
Chromosome Location	chr3:70587736-70587737
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]
rs11918342	0.81[ASN][1000 genomes]
rs11929694	0.81[ASN][1000 genomes]
rs12634194	0.81[ASN][1000 genomes]
rs1491607	0.81[ASN][1000 genomes]
rs1491609	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17790790	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1873566	0.80[ASN][1000 genomes]
rs2172191	0.89[EUR][1000 genomes]
rs55732253	0.83[ASN][1000 genomes]
rs62256300	0.84[ASN][1000 genomes]
rs6549341	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6796357	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7627684	0.80[ASN][1000 genomes]
rs7627883	0.80[ASN][1000 genomes]
rs9849440	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9856709	0.89[ASN][1000 genomes]
rs9871358	0.82[CEU][hapmap];0.85[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70581600-70592000	Weak transcription	H9 Cell Line	embryonic stem cell

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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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