Variant report

Variant	rs6047969
Chromosome Location	chr20:22216601-22216602
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11904956	1.00[AMR][1000 genomes]
rs11908413	1.00[AMR][1000 genomes]
rs6036069	1.00[AMR][1000 genomes]
rs6036078	1.00[AMR][1000 genomes]
rs6047980	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6047981	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6047996	1.00[AMR][1000 genomes]
rs6048002	1.00[AMR][1000 genomes]
rs6048014	1.00[AMR][1000 genomes]
rs6048015	1.00[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	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	nsv1065067	chr20:22199617-22240462	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22214800-22217800	Enhancers	Dnd41	blood
2	chr20:22216600-22217000	Enhancers	Fetal Thymus	thymus

Quick Search:

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

what's new

Quick links