Variant report

Variant	rs4655522
Chromosome Location	chr1:67599764-67599765
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10889665	0.88[EUR][1000 genomes]
rs10889667	0.88[EUR][1000 genomes]
rs10889668	0.81[EUR][1000 genomes]
rs11801083	0.87[EUR][1000 genomes]
rs12069782	0.80[EUR][1000 genomes]
rs12090164	0.80[EUR][1000 genomes]
rs1358748	0.88[EUR][1000 genomes]
rs1358749	0.90[EUR][1000 genomes]
rs1884443	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2064691	0.88[EUR][1000 genomes]
rs2180296	0.91[EUR][1000 genomes]
rs2863203	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3762318	0.80[EUR][1000 genomes]
rs4655521	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4655681	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4655688	0.87[EUR][1000 genomes]
rs4655689	0.86[EUR][1000 genomes]
rs4655690	0.86[EUR][1000 genomes]
rs6588244	1.00[ASN][1000 genomes]
rs6666144	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6683455	0.90[EUR][1000 genomes]
rs6684024	0.90[EUR][1000 genomes]
rs6687620	0.87[EUR][1000 genomes]
rs6703475	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7518757	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7540900	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[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	nsv461751	chr1:67479598-67689036	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv546445	chr1:67479598-67689036	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv461762	chr1:67551209-67648460	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv546446	chr1:67551209-67648460	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv870950	chr1:67575549-67627260	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr1:67585400-67600400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:67592600-67600200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:67598800-67600400	Enhancers	Fetal Intestine Large	intestine
4	chr1:67599200-67600200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:67599200-67600400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:67599400-67600400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:67599600-67602800	Weak transcription	K562	blood

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