Variant report

Variant	rs72991755
Chromosome Location	chr2:141746869-141746870
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1429361	0.81[ASN][1000 genomes]
rs1997077	0.85[EUR][1000 genomes]
rs57278894	0.94[EUR][1000 genomes]
rs58237958	0.94[EUR][1000 genomes]
rs60047991	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60260944	0.98[EUR][1000 genomes]
rs61374054	0.94[EUR][1000 genomes]
rs72975033	0.94[EUR][1000 genomes]
rs72975034	0.94[EUR][1000 genomes]
rs72975037	0.94[EUR][1000 genomes]
rs72975041	0.94[EUR][1000 genomes]
rs72975064	0.89[EUR][1000 genomes]
rs72981063	0.85[EUR][1000 genomes]
rs72991752	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs72991765	0.98[EUR][1000 genomes]
rs72991770	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72991775	0.98[EUR][1000 genomes]
rs7574802	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1003008	chr2:141518795-141763505	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv875208	chr2:141657878-141795620	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1014208	chr2:141707558-141790148	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv817518	chr2:141714174-142287302	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141745600-141747200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:141745600-141747200	Enhancers	HUVEC	blood vessel
3	chr2:141745800-141748200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr2:141746000-141747200	Enhancers	Hela-S3	cervix
5	chr2:141746600-141747000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr2:141746800-141747000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:141746800-141747200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:141746800-141748200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured 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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