Variant report

Variant	rs7596737
Chromosome Location	chr2:64614394-64614395
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10172854	0.95[ASN][1000 genomes]
rs10176971	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10209368	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12470429	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1346236	0.95[ASN][1000 genomes]
rs1365478	0.95[ASN][1000 genomes]
rs1365479	0.95[ASN][1000 genomes]
rs2114433	0.95[ASN][1000 genomes]
rs2162381	0.95[ASN][1000 genomes]
rs2288301	0.95[ASN][1000 genomes]
rs4372888	0.97[ASN][1000 genomes]
rs4508583	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4535030	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4671090	0.95[ASN][1000 genomes]
rs4671567	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4671568	0.95[ASN][1000 genomes]
rs4671569	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4671570	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7578955	0.99[AMR][1000 genomes];0.99[EUR][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	nsv1013132	chr2:64235175-64631084	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1006553	chr2:64339907-64764771	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv834244	chr2:64480943-64646259	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 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	chr2:64595600-64627800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:64610600-64627200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:64613600-64614400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:64613800-64614400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:64613800-64614400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:64613800-64614400	Enhancers	Stomach Mucosa	stomach
7	chr2:64613800-64614800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:64614000-64614400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:64614000-64618800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:64614200-64614400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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