Variant report

Variant	rs6074991
Chromosome Location	chr20:15983080-15983081
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11087157	0.84[EUR][1000 genomes]
rs11087158	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs17711684	0.81[CEU][hapmap]
rs2069316	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs28672081	0.86[ASN][1000 genomes]
rs6074990	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs6074993	0.83[CEU][hapmap]
rs6074994	0.83[CEU][hapmap]
rs6080078	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6080081	0.99[EUR][1000 genomes]
rs6080084	0.83[CEU][hapmap]
rs7352926	0.81[CEU][hapmap]

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	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
3	nsv1065548	chr20:15971797-16023086	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 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	chr20:15959000-15985400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr20:15979000-15985600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr20:15979000-16004200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr20:15982800-15988600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr20:15983000-15983400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr20:15983000-15983400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr20:15983000-15983600	Strong transcription	Primary B cells from cord blood	blood

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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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