Variant report

Variant	rs1000599
Chromosome Location	chr6:44746883-44746884
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]
rs2093346	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs227852	0.84[MKK][hapmap]
rs227853	0.81[YRI][hapmap]
rs56793534	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6905609	1.00[EUR][1000 genomes]
rs6926912	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73734734	1.00[EUR][1000 genomes]
rs73734736	1.00[EUR][1000 genomes]
rs73734737	1.00[EUR][1000 genomes]
rs7770848	1.00[EUR][1000 genomes]
rs7775570	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9463016	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9472333	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9689949	1.00[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44740000-44752000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:44746400-44748200	Enhancers	GM12878-XiMat	blood
3	chr6:44746800-44748000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:44746800-44748200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr6:44746800-44748400	Enhancers	Primary monocytes fromperipheralblood	blood

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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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