Variant report

Variant	rs62194182
Chromosome Location	chr20:15907832-15907833
allele	A/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[AMR][1000 genomes]
rs6074977	0.87[EUR][1000 genomes]
rs6074981	0.93[EUR][1000 genomes]
rs6080009	1.00[AMR][1000 genomes]
rs6080029	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6080033	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6080035	0.85[EUR][1000 genomes]
rs6080037	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6080041	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6080049	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6080053	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6080059	0.93[EUR][1000 genomes]
rs62194163	1.00[AMR][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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15884400-15917400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr20:15904800-15916200	Weak transcription	GM12878-XiMat	blood
3	chr20:15905800-15911000	Weak transcription	Primary B cells from cord blood	blood
4	chr20:15906800-15911200	Weak transcription	HMEC	breast
5	chr20:15907600-15909600	Enhancers	Placenta Amnion	Placenta Amnion

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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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