Variant report

Variant	rs11038602
Chromosome Location	chr11:45662133-45662134
allele	C/T
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]
rs11038595	0.98[ASN][1000 genomes]
rs11038604	0.94[ASN][1000 genomes]
rs11038605	0.80[ASN][1000 genomes]
rs1992849	0.98[ASN][1000 genomes]
rs2277272	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3740702	0.92[ASN][1000 genomes]
rs3802762	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4148898	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4148902	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4148903	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4540819	0.97[ASN][1000 genomes]
rs4755331	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72896778	0.94[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45659200-45669400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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