Variant report

Variant	rs6891047
Chromosome Location	chr5:59622906-59622907
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs16877888	0.87[AMR][1000 genomes]
rs16877890	1.00[AMR][1000 genomes]
rs16877893	1.00[AMR][1000 genomes]
rs16877895	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4460096	1.00[AMR][1000 genomes]
rs57172565	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60693366	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61497235	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6874690	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6875020	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6892680	1.00[AMR][1000 genomes]
rs73104776	1.00[AMR][1000 genomes]
rs73104780	1.00[AMR][1000 genomes]
rs73104781	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106708	1.00[AMR][1000 genomes]
rs73106740	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106742	1.00[AMR][1000 genomes]
rs73106751	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106756	0.85[AMR][1000 genomes]
rs73106759	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106769	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106773	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106774	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106777	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7712352	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7712697	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59619000-59623400	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59620000-59623600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:59620000-59625000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr5:59620400-59629400	Weak transcription	Aorta	Aorta
5	chr5:59620400-59631000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:59622000-59623400	Enhancers	HepG2	liver
7	chr5:59622400-59623200	Enhancers	Stomach Mucosa	stomach
8	chr5:59622800-59623200	Enhancers	Placenta Amnion	Placenta Amnion

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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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