Variant report

Variant	rs72908006
Chromosome Location	chr11:46185542-46185543
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10501317	0.86[ASN][1000 genomes]
rs72906282	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72908007	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908009	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908013	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908014	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908015	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908022	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908033	0.81[ASN][1000 genomes]
rs72908034	0.93[ASN][1000 genomes]
rs72908050	0.86[ASN][1000 genomes]
rs72908052	0.86[ASN][1000 genomes]
rs72908065	0.86[ASN][1000 genomes]
rs72908086	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	chr11:46184600-46192200	Weak transcription	Pancreas	Pancrea
2	chr11:46185400-46185600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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