Variant report

Variant	rs4945084
Chromosome Location	chr11:76121290-76121291
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs4944108	0.91[CEU][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4945083	0.90[CEU][hapmap];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6592632	0.81[CEU][hapmap]
rs6592633	0.99[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7115322	0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7129437	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76097200-76122000	Weak transcription	Fetal Stomach	stomach
2	chr11:76120200-76121600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:76120400-76121800	Weak transcription	Fetal Kidney	kidney

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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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