Variant report

Variant	rs59978141
Chromosome Location	chr6:164244787-164244788
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1111706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895237	1.00[AMR][1000 genomes]
rs16895341	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895371	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895397	0.90[AFR][1000 genomes]
rs16895830	1.00[AMR][1000 genomes]
rs58088941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58323755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58940985	1.00[AMR][1000 genomes]
rs59310825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59525582	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60789865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6455923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6455924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7744004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7744805	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7757701	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7775589	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164230400-164249200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:164236400-164249000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:164243400-164245400	Weak transcription	Brain Germinal Matrix	brain
4	chr6:164243400-164247600	Weak transcription	Fetal Muscle Leg	muscle
5	chr6:164243400-164249000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:164244000-164244800	Bivalent Enhancer	K562	blood
7	chr6:164244000-164247800	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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