Variant report

Variant	rs57666968
Chromosome Location	chr20:23290566-23290567
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11905535	1.00[ASN][1000 genomes]
rs11907155	1.00[ASN][1000 genomes]
rs2405228	1.00[ASN][1000 genomes]
rs56752409	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56848262	1.00[ASN][1000 genomes]
rs57270728	1.00[ASN][1000 genomes]
rs58071233	1.00[ASN][1000 genomes]
rs58496407	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58950746	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs59146474	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs59371748	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs59775607	1.00[ASN][1000 genomes]
rs6036373	1.00[ASN][1000 genomes]
rs6048686	0.98[ASN][1000 genomes]
rs60763856	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61259462	1.00[ASN][1000 genomes]
rs61322006	1.00[ASN][1000 genomes]
rs61594626	1.00[ASN][1000 genomes]
rs7264784	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7267816	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7269309	1.00[ASN][1000 genomes]
rs7270669	1.00[ASN][1000 genomes]
rs7270895	1.00[ASN][1000 genomes]
rs7270957	1.00[ASN][1000 genomes]
rs73316999	1.00[ASN][1000 genomes]
rs73319039	1.00[ASN][1000 genomes]
rs73319041	1.00[ASN][1000 genomes]
rs73904242	1.00[ASN][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	nsv458948	chr20:23234699-23292849	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv585721	chr20:23234699-23292849	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23280000-23291000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr20:23285400-23291600	Weak transcription	Spleen	Spleen
3	chr20:23285600-23301200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr20:23289600-23292000	Weak transcription	K562	blood

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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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