Variant report

Variant	rs6036078
Chromosome Location	chr20:22256357-22256358
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11904956	1.00[AMR][1000 genomes]
rs11908413	1.00[AMR][1000 genomes]
rs6036069	1.00[AMR][1000 genomes]
rs6047969	1.00[AMR][1000 genomes]
rs6047980	1.00[AMR][1000 genomes]
rs6047981	1.00[AMR][1000 genomes]
rs6047996	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6047997	1.00[YRI][hapmap]
rs6047998	1.00[YRI][hapmap]
rs6048001	1.00[AFR][1000 genomes]
rs6048002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6048014	1.00[AMR][1000 genomes]
rs6048015	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1058137	chr20:21549350-22295051	Weak transcription Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv544212	chr20:22233715-22256861	Enhancers Weak transcription	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv962639	chr20:22254826-22283685	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22256200-22257000	Enhancers	Dnd41	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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