Variant report

Variant	rs6135581
Chromosome Location	chr20:15855572-15855573
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs6131735	0.90[ASN][1000 genomes]
rs6131740	1.00[AFR][1000 genomes]
rs6131741	1.00[AFR][1000 genomes]
rs6131749	1.00[AFR][1000 genomes]
rs6135582	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6135583	0.95[ASN][1000 genomes]
rs6135584	0.90[ASN][1000 genomes]
rs6135585	0.90[ASN][1000 genomes]
rs6135586	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6135587	0.89[ASN][1000 genomes]
rs6135588	0.89[ASN][1000 genomes]
rs6135600	1.00[AFR][1000 genomes]
rs6135601	1.00[AFR][1000 genomes]
rs6135603	1.00[AFR][1000 genomes]
rs6135604	1.00[AFR][1000 genomes]
rs6135613	1.00[AFR][1000 genomes]
rs6135614	1.00[AFR][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	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv833929	chr20:15765372-15977337	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3447866	chr20:15799286-16115291	Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island 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	chr20:15840600-15855600	Weak transcription	Primary B cells from cord blood	blood
2	chr20:15850800-15857800	Weak transcription	Spleen	Spleen
3	chr20:15855400-15856600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr20:15855400-15856600	Enhancers	Primary B cells from peripheral blood	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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