Variant report

Variant	rs12679855
Chromosome Location	chr8:20982035-20982036
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10111769	0.81[ASN][1000 genomes]
rs10112502	0.97[ASN][1000 genomes]
rs10503698	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11990863	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11996651	0.87[ASN][1000 genomes]
rs12674821	0.85[ASN][1000 genomes]
rs12675109	0.86[ASN][1000 genomes]
rs12676979	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12677314	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12678981	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12679819	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12680270	0.87[ASN][1000 genomes]
rs12680287	0.88[ASN][1000 genomes]
rs12681224	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1563919	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1563920	0.87[ASN][1000 genomes]
rs1563921	0.87[ASN][1000 genomes]
rs17605964	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1841510	0.93[ASN][1000 genomes]
rs2631894	0.85[ASN][1000 genomes]
rs34133224	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34326138	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34402513	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35089394	0.86[ASN][1000 genomes]
rs35393501	0.83[ASN][1000 genomes]
rs35508548	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35923081	0.86[ASN][1000 genomes]
rs3903353	0.92[ASN][1000 genomes]
rs4739209	0.87[ASN][1000 genomes]
rs4739280	0.83[ASN][1000 genomes]
rs60715093	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7015657	0.89[ASN][1000 genomes]
rs898648	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032450	chr8:20514995-21033577	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv539524	chr8:20514995-21033577	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1034265	chr8:20742935-21152545	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv539528	chr8:20742935-21152545	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv831260	chr8:20907266-21097125	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv469878	chr8:20955260-21128307	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv482339	chr8:20955260-21128307	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 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	chr8:20977600-20983000	Weak transcription	Fetal Muscle Leg	muscle
2	chr8:20981800-20983400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:20981800-20983400	Enhancers	Right Atrium	heart
4	chr8:20981800-20983600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:20981800-20984400	Enhancers	Left Ventricle	heart
6	chr8:20982000-20983400	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:20982000-20984000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:20982000-20989600	Enhancers	Fetal Heart	heart

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