Variant report

Variant	rs6921353
Chromosome Location	chr6:166710791-166710792
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs13204594	0.80[AMR][1000 genomes]
rs1998167	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1998168	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3926288	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4441936	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4710037	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4710038	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4710039	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6456072	0.86[EUR][1000 genomes]
rs6456073	0.92[EUR][1000 genomes]
rs6921526	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7772415	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9295332	0.83[AMR][1000 genomes]
rs9295333	0.83[AMR][1000 genomes]
rs9295335	0.83[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	nsv886934	chr6:166642850-166747572	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv886935	chr6:166704744-166726566	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	4 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	chr6:166706000-166711000	Enhancers	Brain Substantia Nigra	brain
2	chr6:166708200-166712000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:166709400-166711000	Flanking Active TSS	Brain Hippocampus Middle	brain
4	chr6:166709800-166711000	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr6:166710400-166710800	Enhancers	Brain Anterior Caudate	brain
6	chr6:166710400-166710800	Flanking Active TSS	Brain Cingulate Gyrus	brain
7	chr6:166710600-166712000	Weak transcription	Brain Angular Gyrus	brain

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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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