Variant report

Variant	rs6080041
Chromosome Location	chr20:15923984-15923985
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs6074966	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs6074977	0.91[EUR][1000 genomes]
rs6074981	0.97[EUR][1000 genomes]
rs6080009	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs6080029	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6080033	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6080035	0.88[EUR][1000 genomes]
rs6080037	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6080049	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6080053	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6080059	0.97[EUR][1000 genomes]
rs62194163	1.00[AMR][1000 genomes]
rs62194182	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62196574	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	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:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15912000-15930200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr20:15921400-15928000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr20:15922400-15924200	Enhancers	Hela-S3	cervix
4	chr20:15923000-15924000	Weak transcription	Aorta	Aorta
5	chr20:15923000-15924200	Enhancers	HSMM	muscle
6	chr20:15923000-15951200	Weak transcription	Primary B cells from peripheral blood	blood
7	chr20:15923200-15924000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr20:15923200-15930200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr20:15923600-15924000	Strong transcription	Primary B cells from cord blood	blood
10	chr20:15923600-15924200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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